Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:101025769-101025837 | Rare:18 | ||||
chr1:109090673-109090835 | Common:3; Rare:33 | ||||
chr1:110407628-110407809 | Common:2; Rare:83 | ||||
chr1:111140038-111140251 | Common:1; Rare:75 | ||||
chr1:112619112-112619182 | Rare:26 | ||||
chr1:112956190-112956337 | Common:4; Rare:70; Clinvar:6; Clinvar (benign):3 | ||||
chr1:113073096-113073230 | Common:1; Rare:48 | ||||
chr1:114716737-114717060 | Common:4; Rare:120; Clinvar:5; Clinvar (benign):1 | ||||
chr1:117367323-117367500 | Common:4; Rare:59 | ||||
chr1:117929601-117929790 | Rare:51 | ||||
chr1:119140645-119140706 | Rare:21 | ||||
chr1:145918680-145919022 | Common:2; Rare:79 | ||||
chr1:145927482-145927612 | Rare:31 | ||||
chr1:145958007-145958219 | Rare:51 | ||||
chr1:149886678-149886918 | Rare:64 |