| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:1570018-1570178 | Common:1; Rare:49 | ||||
| chr7:2242177-2242263 | Common:2; Rare:50 | ||||
| chr7:2354064-2354111 | Rare:23 | ||||
| chr7:2403314-2403632 | Common:1; Rare:125 | ||||
| chr7:4882181-4882276 | Common:1; Rare:19 | ||||
| chr7:5513768-5513876 | Common:1; Rare:42 | ||||
| chr7:5529763-5530063 | Common:1; Rare:136 | ||||
| chr7:5592668-5592841 | Common:1; Rare:61 | ||||
| chr7:5603301-5603559 | Common:2; Rare:97 | ||||
| chr7:6009029-6009350 | Common:4; Rare:136; Clinvar:3; Clinvar (benign):15 | ||||
| chr7:6401701-6402027 | Rare:63 | ||||
| chr7:6577379-6577513 | Common:1; Rare:45 | ||||
| chr7:7566812-7567051 | Common:4; Rare:95 | ||||
| chr7:10973766-10973948 | Rare:80 | ||||
| chr7:12211128-12211400 | Common:3; Rare:126 |