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GWAS Study

Fine-mapping and cell-specific enrichment at corneal resistance factor loci prioritize candidate causal regulatory variants.

Jiang X, Dellepiane N, Pairo-Castineira E et al.

33311554 PubMed ID
GWAS Study Type
86159 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

JX
Jiang X
DN
Dellepiane N
PE
Pairo-Castineira E
BT
Boutin T
KY
Kumar Y
BW
Bickmore WA
VV
Vitart V
Chapter II

Abstract

Summary of the research findings

Corneal resistance factor (CRF) is altered during corneal diseases progression. Genome-wide-association studies (GWAS) indicated potential CRF and disease genetics overlap. Here, we characterise 135 CRF loci following GWAS in 76029 UK Biobank participants. Enrichment of extra-cellular matrix gene-sets, genetic correlation with corneal thickness (70% (SE = 5%)), reported keratoconus risk variants at 13 loci, all support relevance to corneal stroma biology. Fine-mapping identifies a subset of 55 highly likely causal variants, 91% of which are non-coding. Genomic features enrichments, using all associated variants, also indicate prominent regulatory causal role. We newly established open chromatin landscapes in two widely-used human cornea immortalised cell lines using ATAC-seq. Variants associated with CRF were significantly enriched in regulatory regions from the corneal stroma-derived cell line and enrichment increases to over 5 fold for variants prioritised by fine-mapping-including at GAS7, SMAD3 and COL6A1 loci. Our analysis generates many hypotheses for future functional validation of aetiological mechanisms.

76,029 white-British ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

86159
Total Participants
GWAS
Study Type
Yes
Replicated
10,130 non white-British ancestry individuals
Replication Participants
European
Ancestry
U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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