Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26531220-26531495 | Common:2; Rare:52 | ||||
chr1:26695576-26695792 | Rare:74 | ||||
chr1:26695820-26696159 | Common:1; Rare:101 | ||||
chr1:26696212-26696405 | Common:1; Rare:59; Clinvar:1 | ||||
chr1:26696635-26696671 | Common:2; Rare:14; Clinvar:1; Clinvar (benign):2 | ||||
chr1:26696704-26696921 | Rare:93; Clinvar:2; Clinvar (benign):3 | ||||
chr1:26786946-26787092 | Rare:34 | ||||
chr1:26787664-26787739 | Rare:24 | ||||
chr1:26787839-26788033 | Common:3; Rare:67; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26788129-26788271 | Rare:39 | ||||
chr1:26826561-26826786 | Rare:75 | ||||
chr1:26826982-26827068 | Rare:14 | ||||
chr1:26862820-26863173 | Rare:73 | ||||
chr1:26890145-26890441 | Common:2; Rare:111 | ||||
chr1:26900010-26900256 | Rare:95 |