Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:114780547-114780748 | Rare:78 | ||||
chr1:115089428-115089619 | Common:2; Rare:74 | ||||
chr1:115641702-115642027 | Common:4; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
chr1:116667664-116667857 | Common:1; Rare:71 | ||||
chr1:117060210-117060359 | Common:2; Rare:46 | ||||
chr1:117368225-117368485 | Rare:69 | ||||
chr1:117929560-117929802 | Common:3; Rare:70 | ||||
chr1:119140616-119140743 | Rare:43 | ||||
chr1:119648146-119648350 | Common:3; Rare:74 | ||||
chr1:120069541-120069813 | Common:5; Rare:74 | ||||
chr1:120176343-120176614 | Common:1; Rare:57 | ||||
chr1:144461558-144461685 | Common:5; Rare:56 | ||||
chr1:145823936-145824257 | Rare:115 | ||||
chr1:145918684-145919013 | Common:2; Rare:71 | ||||
chr1:145927394-145927654 | Common:1; Rare:70; Clinvar (pathogenic):1 |