| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:27179833-27179960 | Rare:52 | ||||
| chr7:27185154-27185449 | Common:1; Rare:100 | ||||
| chr7:27200144-27200469 | Common:1; Rare:106 | ||||
| chr7:27740039-27740223 | Common:5; Rare:57 | ||||
| chr7:28409101-28409387 | Common:1; Rare:73 | ||||
| chr7:28685856-28686158 | Common:1; Rare:70 | ||||
| chr7:30026523-30026862 | Rare:82; Clinvar (benign):1 | ||||
| chr7:30028245-30028379 | Rare:31 | ||||
| chr7:30504734-30505103 | Common:3; Rare:124 | ||||
| chr7:30594717-30594983 | Common:4; Rare:125; Clinvar:6; Clinvar (benign):8 | ||||
| chr7:30771304-30771453 | Common:1; Rare:47 | ||||
| chr7:32495247-32495564 | Rare:80 | ||||
| chr7:33062714-33062961 | Common:3; Rare:101 | ||||
| chr7:33109324-33109633 | Common:1; Rare:102; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:35254057-35254225 | Common:1; Rare:58 |