Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26786942-26787058 | Rare:27 | ||||
chr1:26787859-26788237 | Common:3; Rare:111; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26900411-26900553 | Rare:52 | ||||
chr1:26921556-26921869 | Common:3; Rare:99 | ||||
chr1:27322020-27322326 | Common:1; Rare:110 | ||||
chr1:27490044-27490286 | Rare:83 | ||||
chr1:27725758-27726058 | Common:4; Rare:85 | ||||
chr1:27772980-27773290 | Common:1; Rare:107 | ||||
chr1:27830655-27830831 | Common:3; Rare:58 | ||||
chr1:27872393-27872571 | Rare:50 | ||||
chr1:27914513-27914847 | Common:1; Rare:130 | ||||
chr1:28088523-28088796 | Common:3; Rare:87 | ||||
chr1:28232919-28232977 | Rare:24 | ||||
chr1:28232979-28233068 | Common:1; Rare:35 | ||||
chr1:28235963-28236232 | Common:3; Rare:87 |