Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42817009-42817137 | Common:1; Rare:33 | ||||
chr1:42817219-42817494 | Rare:97 | ||||
chr1:42846399-42846635 | Common:1; Rare:66 | ||||
chr1:42958809-42959042 | Common:3; Rare:63; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43172194-43172347 | Common:1; Rare:66 | ||||
chr1:43285519-43285652 | Common:1; Rare:27 | ||||
chr1:43358662-43359006 | Common:7; Rare:110 | ||||
chr1:43367929-43368208 | Rare:71 | ||||
chr1:43386960-43387121 | Rare:27 | ||||
chr1:43389757-43389971 | Common:4; Rare:93; Clinvar:1 | ||||
chr1:43524995-43525199 | Rare:31 | ||||
chr1:43613450-43613654 | Common:1; Rare:51 | ||||
chr1:43946553-43947011 | Rare:130 | ||||
chr1:43974861-43974997 | Common:3; Rare:45 | ||||
chr1:44031399-44031768 | Common:3; Rare:75 |