Multiomic iPSCORE QTLs
This collection contains processed data from "Multiomic QTL mapping reveals phenotypic complexity of GWAS loci and prioritizes putative causal variants" Arthur and Nguyen et al, 2025, Cell Genomics.
In this study, we identified quantitative trait loci (QTLs) that affect gene expression (eQTLs), chromatin accessibility (caQTLs), and histone acetylation (haQTLs), using RNA-seq, ATAC-seq, and H3K27ac ChIP-seq, respectively, generated from induced pluripotent stem cells (iPSCs), and derived cardiovascular progenitor cells (CVPCs), and pancreatic progenitors (PPCs).
There are six items in this collection, including:
1) Summary statistics for the QTL analyses
2) Results from an analysis to identify temporal regulatory variation using mashr
3) Coordinate information for ATAC-seq and H3K27ac ChIP-seq peaks
4) Phenotype count matrices for the eight datasets
5) Bayesian QTL-GWAS Colocalization results
6) Transcription factor predictions in ATAC-seq peaks
Please see the descriptions in the individual items for more detail.
CITE THIS COLLECTION
FUNDING
San Diego Biomedical Informatics Education & Research (SABER)
United States National Library of Medicine
Pancreas cell type-specific regulatory variants and T2D disease risk association
National Institute of Diabetes and Digestive and Kidney Diseases
Functional Analysis of T2D Associated Non-coding SNPs
National Institute of Diabetes and Digestive and Kidney Diseases
Fine-mapping and functional analysis of T1D-associated variants
National Institute of Diabetes and Digestive and Kidney Diseases
Diabetes Research Center (DRC)
National Institute of Diabetes and Digestive and Kidney Diseases
Cardiac stage-specific regulatory variants and their disease risk association
National Heart Lung and Blood Institute
REGULATORY GENOMIC STUDIES IN A COHORT OF IPS CELL DERIVED CARDIOMYOCYTES
National Heart Lung and Blood Institute
Genetic & Social Determinants of Health: Center for Admixture Science and Technology
National Human Genome Research Institute
Optimizing HaploSeq for whole-genome phased haplotypes in biomedical applications
National Human Genome Research Institute
Center of Excellence for Stem Cell Genomics – Salk
California Institute for Regenerative Medicine