Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:116754355-116754483 | Rare:35 | ||||
chr1:117121705-117121971 | Common:1; Rare:82 | ||||
chr1:117367323-117367552 | Common:5; Rare:76 | ||||
chr1:117605768-117606057 | Rare:84 | ||||
chr1:117929560-117929821 | Common:4; Rare:79 | ||||
chr1:118185147-118185356 | Rare:56 | ||||
chr1:119140585-119140785 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:119648136-119648367 | Common:3; Rare:79 | ||||
chr1:120069548-120069969 | Common:7; Rare:84 | ||||
chr1:120176343-120176647 | Common:1; Rare:59 | ||||
chr1:120914087-120914192 | Rare:10 | ||||
chr1:121087146-121087368 | Rare:41 | ||||
chr1:121184826-121185088 | Rare:89 | ||||
chr1:121185185-121185368 | Rare:29 | ||||
chr1:145214680-145215034 | Rare:38 |