Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42846392-42846636 | Common:1; Rare:68 | ||||
chr1:42958821-42959042 | Common:3; Rare:61; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43358674-43359090 | Common:7; Rare:128 | ||||
chr1:43367975-43368124 | Rare:40 | ||||
chr1:43389757-43389945 | Common:3; Rare:83 | ||||
chr1:44674413-44674714 | Common:3; Rare:84 | ||||
chr1:44739658-44739949 | Common:2; Rare:116 | ||||
chr1:44775480-44775613 | Rare:54 | ||||
chr1:45339996-45340227 | Rare:83; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:45499998-45500335 | Common:2; Rare:75; Clinvar:4; Clinvar (pathogenic):2 | ||||
chr1:45521827-45522064 | Common:1; Rare:95 | ||||
chr1:45522841-45522890 | Rare:7 | ||||
chr1:45686471-45686653 | Rare:65 | ||||
chr1:45687036-45687274 | Common:2; Rare:71 | ||||
chr1:45688055-45688211 | Common:1; Rare:39 |