Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111139720-111139744 | Not yet | Rare:4 | 19 | ||
chr1:111140037-111140294 | Not yet | Common:2; Rare:89 | 266 | ||
chr1:111200119-111200326 | Not yet | Common:3; Rare:30 | 341 | ||
chr1:111200629-111200762 | Not yet | Rare:31 | 189 | ||
chr1:111346525-111346650 | Not yet | Common:1; Rare:35 | 204 | ||
chr1:111739361-111739560 | Not yet | Common:2; Rare:51 | 250 | ||
chr1:112396022-112396258 | Not yet | Common:1; Rare:73 | 214 | ||
chr1:112619099-112619199 | Not yet | Rare:36 | 153 | ||
chr1:112619642-112619871 | Not yet | Common:1; Rare:83 | 242 | ||
chr1:112707080-112707222 | Not yet | Rare:48 | 141 | ||
chr1:112956188-112956437 | Not yet | Common:4; Rare:114; Clinvar:9; Clinvar (benign):3 | 203 | ||
chr1:113073105-113073221 | Not yet | Common:1; Rare:43 | 180 | ||
chr1:113390145-113390523 | Not yet | Common:2; Rare:94 | 266 | ||
chr1:113812241-113812571 | Not yet | Common:2; Rare:136 | 350 | ||
chr1:113904824-113905344 | Not yet | Common:5; Rare:154; Clinvar (benign):1 | 372 |