| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:7566803-7567037 | Common:4; Rare:96 | ||||
| chr7:16645631-16645976 | Rare:110 | ||||
| chr7:19117634-19117960 | Common:1; Rare:75 | ||||
| chr7:22726984-22727240 | Common:2; Rare:34 | ||||
| chr7:23105663-23105839 | Common:4; Rare:94; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181914-23182128 | Rare:93 | ||||
| chr7:26200705-26201108 | Common:1; Rare:193 | ||||
| chr7:26201277-26201550 | Rare:100 | ||||
| chr7:26201590-26201824 | Common:2; Rare:122 | ||||
| chr7:27096000-27096144 | Rare:42 | ||||
| chr7:27185050-27185433 | Common:1; Rare:119 | ||||
| chr7:27740073-27740202 | Common:4; Rare:32 | ||||
| chr7:30594714-30595134 | Common:7; Rare:187; Clinvar:11; Clinvar (benign):15 | ||||
| chr7:33062718-33062871 | Common:1; Rare:74 | ||||
| chr7:33109331-33109513 | Rare:68; Clinvar:1; Clinvar (benign):1 |