Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111346543-111346650 | Rare:31 | ||||
chr1:111739374-111739560 | Common:2; Rare:48 | ||||
chr1:112395981-112396267 | Common:1; Rare:90 | ||||
chr1:112619105-112619236 | Rare:46 | ||||
chr1:112619643-112619851 | Common:1; Rare:71 | ||||
chr1:112956169-112956467 | Common:5; Rare:129; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073081-113073221 | Common:1; Rare:47 | ||||
chr1:113390143-113390519 | Common:2; Rare:94 | ||||
chr1:113759120-113759194 | Rare:18 | ||||
chr1:113812192-113812623 | Common:3; Rare:174 | ||||
chr1:113905010-113905399 | Common:5; Rare:113 | ||||
chr1:114152914-114153012 | Common:2; Rare:29 | ||||
chr1:114581572-114581817 | Common:1; Rare:113 | ||||
chr1:114716701-114716826 | Rare:53; Clinvar:3 | ||||
chr1:114757925-114758112 | Common:3; Rare:62 |