Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111739358-111739548 | Common:1; Rare:47 | ||||
chr1:112396003-112396267 | Common:1; Rare:83 | ||||
chr1:112619109-112619205 | Rare:33 | ||||
chr1:112619642-112619746 | Rare:31 | ||||
chr1:112619748-112619856 | Common:1; Rare:43 | ||||
chr1:112707080-112707483 | Common:1; Rare:124 | ||||
chr1:112956165-112956467 | Common:5; Rare:130; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073095-113073230 | Common:1; Rare:48 | ||||
chr1:113390185-113390512 | Common:1; Rare:82 | ||||
chr1:113812232-113812579 | Common:2; Rare:141 | ||||
chr1:113905010-113905365 | Common:3; Rare:102 | ||||
chr1:113979568-113979622 | Rare:13 | ||||
chr1:114581584-114581818 | Rare:104 | ||||
chr1:115089415-115089606 | Common:2; Rare:74 | ||||
chr1:115641811-115642032 | Common:3; Rare:76; Clinvar:1; Clinvar (benign):2 |