| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:18821294-18821382 | Common:1; Rare:14 | ||||
| chr7:18821433-18821506 | Common:3; Rare:17 | ||||
| chr7:18821513-18821711 | Common:7; Rare:45 | ||||
| chr7:20560713-20560865 | Common:2; Rare:52 | ||||
| chr7:23036171-23036298 | Common:2; Rare:29 | ||||
| chr7:23471101-23471525 | Common:2; Rare:118 | ||||
| chr7:23474349-23474946 | Common:1; Rare:174 | ||||
| chr7:23490417-23490631 | Common:3; Rare:102 | ||||
| chr7:23680805-23681035 | Common:3; Rare:51 | ||||
| chr7:24214810-24214961 | Rare:24 | ||||
| chr7:24504949-24505014 | Common:1; Rare:6 | ||||
| chr7:25855113-25855342 | Rare:53 | ||||
| chr7:25856959-25857273 | Common:12; Rare:91 | ||||
| chr7:26193249-26193696 | Rare:156; Clinvar (benign):2 | ||||
| chr7:26376021-26376464 | Common:6; Rare:123 |