| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:170554211-170554412 | Common:1; Rare:65 | ||||
| chr7:727235-727303 | Rare:22; Clinvar:1 | ||||
| chr7:1138213-1138409 | Common:2; Rare:57 | ||||
| chr7:1538076-1538297 | Common:1; Rare:72 | ||||
| chr7:1570007-1570146 | Common:1; Rare:45 | ||||
| chr7:1940479-1940669 | Rare:58 | ||||
| chr7:2242152-2242270 | Common:2; Rare:73 | ||||
| chr7:5045783-5045872 | Common:2; Rare:43 | ||||
| chr7:5513742-5513886 | Common:1; Rare:63 | ||||
| chr7:6009021-6009361 | Common:4; Rare:146; Clinvar:9; Clinvar (benign):15 | ||||
| chr7:6104627-6104946 | Common:5; Rare:121 | ||||
| chr7:6272560-6272754 | Rare:93 | ||||
| chr7:6447919-6448034 | Rare:44 | ||||
| chr7:6483972-6484277 | Common:2; Rare:135 | ||||
| chr7:7566767-7567047 | Common:5; Rare:114 |