Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24642890-24643335 | Common:2; Rare:147 | ||||
chr1:25232425-25232650 | Rare:91 | ||||
chr1:25247435-25247691 | Common:4; Rare:93 | ||||
chr1:25338180-25338486 | Common:2; Rare:104 | ||||
chr1:25819919-25820029 | Common:2; Rare:32 | ||||
chr1:26279941-26280203 | Rare:144 | ||||
chr1:26432162-26432415 | Common:4; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472314-26472544 | Common:4; Rare:86 | ||||
chr1:26890229-26890377 | Common:1; Rare:61 | ||||
chr1:26900438-26900482 | Rare:18 | ||||
chr1:26921522-26921832 | Common:3; Rare:97 | ||||
chr1:27725690-27725996 | Common:2; Rare:89 | ||||
chr1:28088541-28088807 | Common:3; Rare:90 | ||||
chr1:28235987-28236209 | Common:3; Rare:74 | ||||
chr1:28328967-28329073 | Rare:27 |