| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:23014031-23014373 | Common:5; Rare:123; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:23105636-23105890 | Common:4; Rare:128; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:23181914-23182128 | Rare:93 | ||||
| chr7:23299227-23299598 | Common:2; Rare:191 | ||||
| chr7:23347680-23347934 | Rare:68 | ||||
| chr7:23470306-23470635 | Common:1; Rare:97 | ||||
| chr7:23531948-23532141 | Common:2; Rare:77 | ||||
| chr7:23597261-23597412 | Rare:47 | ||||
| chr7:23679994-23680203 | Common:5; Rare:61 | ||||
| chr7:23722629-23722827 | Common:1; Rare:37 | ||||
| chr7:24757406-24757640 | Common:1; Rare:68 | ||||
| chr7:24980108-24980425 | Common:8; Rare:132 | ||||
| chr7:25125191-25125643 | Rare:182; Clinvar:3 | ||||
| chr7:26200190-26200358 | Common:2; Rare:81 | ||||
| chr7:26200564-26200945 | Common:2; Rare:184 |