| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:142943913-142944078 | Common:2; Rare:29 | ||||
| chr6:142946230-142946558 | Common:2; Rare:78 | ||||
| chr6:155106858-155107057 | Rare:29 | ||||
| chr6:155253834-155254006 | Rare:37 | ||||
| chr6:157380004-157380204 | Common:3; Rare:42 | ||||
| chr6:169790277-169790379 | Common:1; Rare:38 | ||||
| chr7:149141-149272 | Common:2; Rare:48 | ||||
| chr7:5427071-5427322 | Common:13; Rare:112 | ||||
| chr7:5427821-5427911 | Rare:33 | ||||
| chr7:5570146-5570344 | Common:2; Rare:68 | ||||
| chr7:5823046-5823295 | Common:4; Rare:97 | ||||
| chr7:6729692-6729807 | Common:1; Rare:48 | ||||
| chr7:22563330-22563377 | Rare:16 | ||||
| chr7:23680815-23681035 | Common:3; Rare:50 | ||||
| chr7:26193252-26193672 | Rare:147; Clinvar (benign):1 |