| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:11272906-11273238 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:11654680-11654901 | Common:4; Rare:63 | ||||
| chr1:11664014-11664227 | Common:2; Rare:56 | ||||
| chr1:11805905-11806204 | Common:2; Rare:81; Clinvar:1 | ||||
| chr1:13749096-13749451 | Common:2; Rare:124 | ||||
| chr1:15410227-15410251 | Rare:4 | ||||
| chr1:15526589-15526905 | Common:2; Rare:99 | ||||
| chr1:15563722-15563870 | Common:6; Rare:23 | ||||
| chr1:19210251-19210405 | Rare:62 | ||||
| chr1:19251522-19251848 | Common:6; Rare:103 | ||||
| chr1:19312080-19312333 | Common:6; Rare:122 | ||||
| chr1:19485437-19485780 | Common:1; Rare:127 | ||||
| chr1:19596657-19597178 | Common:5; Rare:177 | ||||
| chr1:20661352-20661687 | Common:3; Rare:121; Clinvar:4; Clinvar (benign):6 | ||||
| chr1:21176848-21177153 | Common:1; Rare:91 |