| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:2242171-2242256 | Common:2; Rare:51 | ||||
| chr7:4775373-4775652 | Common:7; Rare:122; Clinvar:1 | ||||
| chr7:5513746-5513844 | Common:1; Rare:46 | ||||
| chr7:6009029-6009355 | Common:4; Rare:137; Clinvar:3; Clinvar (benign):15 | ||||
| chr7:6104626-6105002 | Common:5; Rare:135 | ||||
| chr7:6484058-6484263 | Common:1; Rare:109 | ||||
| chr7:7566767-7567047 | Common:5; Rare:114 | ||||
| chr7:12686733-12686913 | Common:2; Rare:56 | ||||
| chr7:16645776-16646122 | Common:2; Rare:109 | ||||
| chr7:17298454-17298682 | Common:3; Rare:59 | ||||
| chr7:17940449-17940549 | Common:1; Rare:51 | ||||
| chr7:18509121-18509369 | Rare:48 | ||||
| chr7:20330567-20330737 | Common:2; Rare:40 | ||||
| chr7:20331754-20331813 | Common:1; Rare:21 | ||||
| chr7:21427845-21428104 | Common:1; Rare:97 |