Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:109548507-109548682 | Common:4; Rare:63 | ||||
chr1:109656016-109656132 | Common:2; Rare:44 | ||||
chr1:110339156-110339452 | Common:1; Rare:84 | ||||
chr1:110407604-110407845 | Common:4; Rare:102 | ||||
chr1:111139804-111139870 | Rare:8 | ||||
chr1:111140036-111140287 | Common:2; Rare:87 | ||||
chr1:111739361-111739704 | Common:3; Rare:96 | ||||
chr1:112396086-112396265 | Common:1; Rare:55 | ||||
chr1:112619109-112619236 | Rare:45 | ||||
chr1:112619685-112619851 | Common:1; Rare:58 | ||||
chr1:112956150-112956393 | Common:4; Rare:103; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113073085-113073221 | Common:1; Rare:46 | ||||
chr1:113905032-113905344 | Common:3; Rare:84 | ||||
chr1:114581587-114581917 | Rare:130 | ||||
chr1:114670004-114670184 | Rare:56 |