Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150560846-150561215 | Common:1; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
chr1:150561258-150561730 | Common:1; Rare:123 | ||||
chr1:150562014-150562309 | Rare:55 | ||||
chr1:150567638-150567930 | Common:1; Rare:60 | ||||
chr1:150568215-150568559 | Rare:79 | ||||
chr1:150577317-150577371 | Common:1; Rare:11 | ||||
chr1:150604777-150605029 | Common:1; Rare:41 | ||||
chr1:150875912-150875993 | Rare:20 | ||||
chr1:150973618-150973708 | Rare:21 | ||||
chr1:150981245-150981459 | Rare:33 | ||||
chr1:151009158-151009339 | Rare:25 | ||||
chr1:151013047-151013391 | Common:1; Rare:58 | ||||
chr1:151013630-151013699 | Rare:14 | ||||
chr1:151055350-151055460 | Common:2; Rare:19 | ||||
chr1:151058733-151058913 | Common:1; Rare:24 |