| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:1138198-1138461 | Common:2; Rare:82 | ||||
| chr7:1570013-1570094 | Common:1; Rare:25 | ||||
| chr7:2242168-2242263 | Common:2; Rare:58 | ||||
| chr7:2403288-2403611 | Common:1; Rare:127 | ||||
| chr7:4775478-4775652 | Common:6; Rare:74; Clinvar:1 | ||||
| chr7:5513746-5513855 | Common:1; Rare:52 | ||||
| chr7:6009029-6009372 | Common:4; Rare:142; Clinvar:4; Clinvar (benign):15 | ||||
| chr7:6104627-6104934 | Common:5; Rare:117 | ||||
| chr7:6483985-6484233 | Common:2; Rare:118 | ||||
| chr7:7182369-7182689 | Common:3; Rare:117 | ||||
| chr7:7566995-7567037 | Rare:16 | ||||
| chr7:8262024-8262291 | Rare:109 | ||||
| chr7:12210967-12211396 | Common:4; Rare:162 | ||||
| chr7:12687389-12687636 | Common:5; Rare:79 | ||||
| chr7:16645694-16646206 | Common:3; Rare:182 |