| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:24699242-24699381 | Rare:39; Clinvar:1 | ||||
| chr7:26188697-26188736 | Rare:10 | ||||
| chr7:26193252-26193695 | Rare:156; Clinvar (benign):2 | ||||
| chr7:27122373-27122545 | Rare:36 | ||||
| chr7:29480680-29481028 | Common:4; Rare:63 | ||||
| chr7:29510266-29510481 | Common:5; Rare:46 | ||||
| chr7:29685618-29685930 | Common:8; Rare:60 | ||||
| chr7:32572924-32573270 | Common:3; Rare:74 | ||||
| chr7:32728050-32728145 | Common:1; Rare:34 | ||||
| chr7:32728568-32728823 | Common:9; Rare:81 | ||||
| chr7:32754717-32754760 | Common:1; Rare:5 | ||||
| chr7:32991554-32991678 | Rare:22 | ||||
| chr7:38358391-38358480 | Common:1; Rare:44 | ||||
| chr7:39733563-39733641 | Rare:21 | ||||
| chr7:42888671-42888978 | Common:1; Rare:68 |