| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:1570007-1570094 | Common:1; Rare:27 | ||||
| chr7:2242171-2242268 | Common:2; Rare:57 | ||||
| chr7:2314353-2314630 | Common:5; Rare:110 | ||||
| chr7:2403278-2403583 | Common:1; Rare:115 | ||||
| chr7:4775485-4775652 | Common:6; Rare:71; Clinvar:1 | ||||
| chr7:5513774-5513844 | Common:1; Rare:32 | ||||
| chr7:5898645-5898792 | Common:4; Rare:30 | ||||
| chr7:6009029-6009355 | Common:4; Rare:137; Clinvar:3; Clinvar (benign):15 | ||||
| chr7:6104626-6104934 | Common:5; Rare:118 | ||||
| chr7:6484038-6484290 | Common:2; Rare:122 | ||||
| chr7:6577402-6577495 | Rare:32 | ||||
| chr7:6826203-6826340 | Common:4; Rare:30 | ||||
| chr7:7182344-7182686 | Common:4; Rare:128 | ||||
| chr7:7566761-7566993 | Common:5; Rare:99 | ||||
| chr7:10940117-10940230 | Rare:44 |