| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:20206522-20206711 | Common:2; Rare:31 | ||||
| chr7:23490411-23490550 | Common:3; Rare:58 | ||||
| chr7:23680805-23680865 | Rare:15 | ||||
| chr7:25662929-25663061 | Common:1; Rare:23 | ||||
| chr7:25750806-25750895 | Rare:10 | ||||
| chr7:25951307-25951543 | Common:2; Rare:64 | ||||
| chr7:26181125-26181350 | Common:2; Rare:79 | ||||
| chr7:26187974-26188098 | Common:2; Rare:58 | ||||
| chr7:26189498-26189512 | Rare:4 | ||||
| chr7:26193252-26193701 | Rare:157; Clinvar (benign):2 | ||||
| chr7:26198348-26198874 | Common:6; Rare:186 | ||||
| chr7:26199271-26199635 | Common:2; Rare:147 | ||||
| chr7:26199922-26199990 | Rare:33 | ||||
| chr7:26199993-26200084 | Common:1; Rare:40 | ||||
| chr7:26399432-26399535 | Common:1; Rare:16 |