| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99552075-99552182 | Rare:39 | ||||
| chr7:99558519-99558870 | Common:3; Rare:102 | ||||
| chr7:99919513-99919640 | Rare:42 | ||||
| chr7:100015470-100015673 | Common:1; Rare:56 | ||||
| chr7:100088889-100089060 | Common:1; Rare:56 | ||||
| chr7:100101316-100101711 | Common:1; Rare:156; Clinvar (benign):1 | ||||
| chr7:100119278-100119731 | Rare:142; Clinvar:1 | ||||
| chr7:100148687-100149017 | Common:1; Rare:144 | ||||
| chr7:100177845-100177964 | Rare:29 | ||||
| chr7:100428227-100428333 | Rare:34 | ||||
| chr7:100428633-100428793 | Common:3; Rare:61 | ||||
| chr7:100429186-100429426 | Common:3; Rare:101 | ||||
| chr7:100436139-100436191 | Common:1; Rare:15 | ||||
| chr7:100436455-100436511 | Rare:19 | ||||
| chr7:100478919-100478965 | Rare:8 |