| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66921102-66921428 | Common:1; Rare:95 | ||||
| chr7:66996569-66996932 | Common:2; Rare:82 | ||||
| chr7:72828136-72828483 | Common:1; Rare:97 | ||||
| chr7:73308786-73308884 | Rare:41 | ||||
| chr7:73683415-73683668 | Common:3; Rare:113 | ||||
| chr7:73738786-73739024 | Common:1; Rare:69 | ||||
| chr7:73842506-73842693 | Common:6; Rare:27 | ||||
| chr7:74174114-74174441 | Common:1; Rare:158 | ||||
| chr7:74254309-74254535 | Rare:106 | ||||
| chr7:74657459-74657731 | Common:2; Rare:80 | ||||
| chr7:74657932-74658067 | Common:1; Rare:31 | ||||
| chr7:75486226-75486458 | Common:2; Rare:86 | ||||
| chr7:75878826-75879101 | Common:12; Rare:101 | ||||
| chr7:75914911-75915164 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994507-75994772 | Common:4; Rare:133 |