| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:11099740-11099921 | Common:2; Rare:76 | ||||
| chr1:11262490-11262903 | Common:3; Rare:122 | ||||
| chr1:11478846-11479174 | Common:6; Rare:96 | ||||
| chr1:11654816-11654931 | Common:2; Rare:33 | ||||
| chr1:11664068-11664205 | Common:1; Rare:38 | ||||
| chr1:11691446-11691769 | Common:4; Rare:74 | ||||
| chr1:11691771-11691862 | Rare:13 | ||||
| chr1:11805918-11806276 | Common:2; Rare:95; Clinvar:1 | ||||
| chr1:11980081-11980473 | Common:6; Rare:125; Clinvar:1; Clinvar (benign):4 | ||||
| chr1:13700175-13700285 | Rare:47 | ||||
| chr1:13749148-13749481 | Common:2; Rare:122 | ||||
| chr1:14598391-14598867 | Common:4; Rare:140 | ||||
| chr1:15524231-15524624 | Common:3; Rare:94 | ||||
| chr1:15526550-15526913 | Common:2; Rare:117 | ||||
| chr1:15758484-15758817 | Common:1; Rare:69 |