| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:26201574-26201815 | Common:2; Rare:125 | ||||
| chr7:26864562-26864855 | Common:3; Rare:93 | ||||
| chr7:27095948-27096198 | Rare:72 | ||||
| chr7:27152533-27152738 | Rare:37 | ||||
| chr7:27179840-27179978 | Rare:50 | ||||
| chr7:27185228-27185391 | Common:1; Rare:68 | ||||
| chr7:27662778-27663178 | Common:6; Rare:141 | ||||
| chr7:27740042-27740209 | Common:5; Rare:46 | ||||
| chr7:28409194-28409391 | Common:1; Rare:50 | ||||
| chr7:30284433-30284745 | Common:5; Rare:128 | ||||
| chr7:30478681-30478924 | Common:4; Rare:84; Clinvar:1 | ||||
| chr7:30504751-30505085 | Common:2; Rare:111 | ||||
| chr7:30594711-30594996 | Common:5; Rare:133; Clinvar:6; Clinvar (benign):10 | ||||
| chr7:32495247-32495617 | Common:1; Rare:93 | ||||
| chr7:33109308-33109521 | Rare:76; Clinvar:1; Clinvar (benign):1 |