Dataset ID
NHA000163
- Type of data
- Fine-mapping for 79 phenotypes
- Access criteria
- Unrestricted-access
- Total data volume
- 4.1 GB
- File formats
- HTML
- ZIP
- Research
- hum0197
- Date published
- 2021-12-21
- Date modified
- 2021-12-21
- Secondary ID
- hum0197.v5.finemap.v1
Unrestricted-access files linked to this dataset
| File | Label | Size | Copy URL |
|---|---|---|---|
| hum0197.v5.finemap.AD.v1.zip | Disease name: Atopic dermatitis / Abbreviation: AD / ICD10: L20 | 19.3 MB | |
| hum0197.v5.finemap.AF.v1.zip | Disease name: Atrial fibrillation / Abbreviation: AFib / ICD10: I48 | 35.0 MB | |
| hum0197.v5.finemap.AG.v1.zip | Disease name: Albumin/Globulin ratio / Abbreviation: AG | 70.7 MB | |
| hum0197.v5.finemap.AID.v1.zip | Disease name: Autoimmune disease / Abbreviation: AID / ICD10: M35 | 11.9 MB | |
| hum0197.v5.finemap.ALP.v1.zip | Disease name: Alkaline phosphatase / Abbreviation: ALP | 55.3 MB | |
| hum0197.v5.finemap.ALT.v2.zip | Disease name: Alanine aminotransferase / Abbreviation: ALT / v2: replaced with the fixed files | 43.9 MB | |
| hum0197.v5.finemap.AST.v2.zip | Disease name: Aspartate aminotransferase / Abbreviation: AST / v2: replaced with the fixed files | 49.2 MB | |
| hum0197.v5.finemap.Alb.v1.zip | Disease name: Albumin / Abbreviation: Alb | 32.1 MB | |
| hum0197.v5.finemap.As.v1.zip | Disease name: Asthma / Abbreviation: Asthma / ICD10: J45 | 26.9 MB | |
| hum0197.v5.finemap.BAS.v1.zip | Disease name: Basophil / Abbreviation: Baso | 51.1 MB | |
| hum0197.v5.finemap.BC.v1.zip | Disease name: Breast cancer / Abbreviation: BrC / ICD10: C50 | 11.4 MB | |
| hum0197.v5.finemap.BMI.v1.zip | Disease name: Body mass index / Abbreviation: BMI | 125 MB | |
| hum0197.v5.finemap.BUN.v1.zip | Disease name: Blood urea nitrogen / Abbreviation: BUN | 56.8 MB | |
| hum0197.v5.finemap.BW.v1.zip | Disease name: Body weight / Abbreviation: BW | 220 MB | |
| hum0197.v5.finemap.CAD.v1.zip | Disease name: Coronary artery disease / Abbreviation: CAD / ICD10: I200、I209、I219 | 74.3 MB | |
| hum0197.v5.finemap.CC.v1.zip | Disease name: Colorectal cancer / Abbreviation: CRC / ICD10: C18 | 20.4 MB | |
| hum0197.v5.finemap.CL.v1.zip | Disease name: Cholelithiasis / Abbreviation: Cholelithiasis / ICD10: K80 | 20.6 MB | |
| hum0197.v5.finemap.COPD.v1.zip | Disease name: Chronic obstructive pulmonary disease / Abbreviation: COPD / ICD10: J44 | 7.6 MB | |
| hum0197.v5.finemap.CRP.v1.zip | Disease name: C-reactive protein / Abbreviation: CRP | 8.5 MB | |
| hum0197.v5.finemap.Ca.v1.zip | Disease name: Calcium / Abbreviation: Ca | 23.3 MB |
1–20 / 80
Analysis method
genome wide SNPs
- Materials and participants
- Biobank Japan (n = 179,000), no. Phenotypes: 79
- Health statusMixed
- Subject count179,000 (Individual)
- CohortBioBank Japan
- Sample description
- DNAs extracted from peripheral blood cells
- TissuePeripheral blood
- Tumor / normalNormal
- Sample provider
- N/A
- Experimental method
- Genotyping by array
- Target
- N/A
- Reagent kit
- HumanExome BeadChip Kit
HumanOmniExpress BeadChip Kit
HumanOmniExpressExome BeadChip Kit - Platform
- Illumina HumanExome
Illumina HumanOmniExpress
Illumina HumanOmniExpressExome - Reference genome
- GRCh37
- QC and filtering
- GWAS: We included imputed variants with Rsq > 0.7. For binary traits, variants with MAC < 10 were additionally excluded.
Fine-mapping: We defined fine-mapping regions based on a 3 Mb window around each lead variant and merged regions if they overlapped. We excluded the major histocompatibility complex (MHC) region (chr 6: 25-36 Mb) from analysis due to extensive LD structure in the region. For each method, we only included variants from successfully fine-mapped regions while excluding those from failed regions (e.g., due to conversion failure or available memory restrictions). - Imputation
- Eagle, Minimac3
- Analysis method
- GWAS: For binary traits, SAIGE software was used with age, age2, sex, age×sex, age2×sex, and top 20 principal components as covariates. For quantitative traits (biomarkers), BOLT-LMM was used with the same covariates.
Fine-mapping: FINEMAP and SuSiE were used with GWAS summary statistics and in-sample dosage LD, allowing up to 10 causal variants per region. - Variant count
- 13,531,752 variants
- Phenotype data
- Included
- Data use policy
- NBDC data sharing policy (JGAP000001)