| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:19117633-19117941 | Common:1; Rare:70 | ||||
| chr7:23105673-23105839 | Common:3; Rare:88; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181929-23182186 | Rare:112 | ||||
| chr7:23470326-23470608 | Common:1; Rare:82 | ||||
| chr7:24757399-24757530 | Common:2; Rare:36 | ||||
| chr7:26196557-26196966 | Common:2; Rare:149; Clinvar (benign):1 | ||||
| chr7:26197315-26197650 | Common:1; Rare:121; Clinvar (benign):1 | ||||
| chr7:26201200-26201477 | Rare:111 | ||||
| chr7:26201619-26201826 | Common:1; Rare:107 | ||||
| chr7:27095990-27096170 | Rare:50 | ||||
| chr7:27113839-27113911 | Rare:18 | ||||
| chr7:27185196-27185428 | Common:1; Rare:84 | ||||
| chr7:27740099-27740202 | Common:3; Rare:28 | ||||
| chr7:30504717-30505068 | Common:3; Rare:119 | ||||
| chr7:30594716-30595119 | Common:6; Rare:182; Clinvar:11; Clinvar (benign):14 |