Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:101843519-101843650 | Common:1; Rare:34 | ||||
chr10:102432546-102432781 | Common:1; Rare:68 | ||||
chr10:102714278-102714627 | Common:2; Rare:117 | ||||
chr10:102776078-102776257 | Common:1; Rare:29 | ||||
chr10:103193240-103193397 | Common:5; Rare:49; Clinvar (benign):1 | ||||
chr10:103396395-103396709 | Rare:113 | ||||
chr10:104121896-104122171 | Common:2; Rare:88 | ||||
chr10:104254822-104254981 | Common:1; Rare:48 | ||||
chr10:104268980-104269190 | Common:2; Rare:48 | ||||
chr10:110007684-110008023 | Rare:102 | ||||
chr10:110919336-110919636 | Common:7; Rare:82 | ||||
chr10:112446877-112447293 | Common:3; Rare:105 | ||||
chr10:113854392-113854964 | Common:1; Rare:137 | ||||
chr10:113854995-113855046 | Rare:18 | ||||
chr10:114821655-114821996 | Common:1; Rare:109 |