Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113929411-113929654 | Common:1; Rare:75 | ||||
chr1:113930662-113930840 | Common:1; Rare:34 | ||||
chr1:113979323-113979576 | Rare:70 | ||||
chr1:114581606-114581797 | Rare:83 | ||||
chr1:114670025-114670178 | Rare:49 | ||||
chr1:114716657-114716990 | Common:4; Rare:126; Clinvar:5; Clinvar (benign):3 | ||||
chr1:116373333-116373521 | Common:3; Rare:59 | ||||
chr1:116386831-116386869 | Rare:7 | ||||
chr1:116571002-116571174 | Common:2; Rare:50 | ||||
chr1:117060180-117060347 | Common:2; Rare:41 | ||||
chr1:117367297-117367531 | Common:5; Rare:85 | ||||
chr1:117367620-117367817 | Rare:42 | ||||
chr1:117368228-117368432 | Rare:50 | ||||
chr1:117929581-117929827 | Common:4; Rare:75 | ||||
chr1:119140621-119140735 | Rare:37 |