Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:109548486-109548707 | Common:4; Rare:83 | ||||
chr1:109656190-109656232 | Rare:5 | ||||
chr1:109656237-109656369 | Rare:30 | ||||
chr1:110390976-110391246 | Rare:52 | ||||
chr1:110407604-110407845 | Common:4; Rare:102 | ||||
chr1:111139424-111139512 | Common:1; Rare:20 | ||||
chr1:111140036-111140292 | Common:2; Rare:89 | ||||
chr1:111346527-111346655 | Rare:37 | ||||
chr1:111739331-111739561 | Common:3; Rare:59 | ||||
chr1:112619109-112619236 | Rare:45 | ||||
chr1:112619643-112619856 | Common:1; Rare:74 | ||||
chr1:112699710-112699936 | Common:1; Rare:67 | ||||
chr1:112956150-112956513 | Common:5; Rare:150; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113073080-113073238 | Common:1; Rare:56 | ||||
chr1:113390218-113390532 | Common:1; Rare:78 |