| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:12686685-12686978 | Common:3; Rare:98 | ||||
| chr7:16753522-16753795 | Rare:96 | ||||
| chr7:17298444-17298659 | Common:3; Rare:54 | ||||
| chr7:17299111-17299236 | Rare:33 | ||||
| chr7:17940454-17940574 | Common:1; Rare:54 | ||||
| chr7:20217352-20217583 | Common:1; Rare:51 | ||||
| chr7:20331681-20331840 | Common:2; Rare:48 | ||||
| chr7:22822724-22822967 | Common:3; Rare:91 | ||||
| chr7:23105673-23105822 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181872-23182189 | Rare:136 | ||||
| chr7:23531954-23532091 | Common:1; Rare:55 | ||||
| chr7:25125238-25125662 | Rare:165; Clinvar:3 | ||||
| chr7:26196370-26197011 | Common:3; Rare:243; Clinvar (benign):5 | ||||
| chr7:26200564-26200847 | Common:1; Rare:145 | ||||
| chr7:26201376-26201555 | Rare:66 |