| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:92134291-92134550 | Rare:79 | ||||
| chr7:92134709-92134899 | Common:3; Rare:57 | ||||
| chr7:92245849-92245970 | Rare:35; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92246099-92246358 | Common:3; Rare:77 | ||||
| chr7:92528370-92528816 | Common:3; Rare:137; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590047-92590170 | Common:1; Rare:49 | ||||
| chr7:92836176-92836498 | Rare:54 | ||||
| chr7:92836540-92836598 | Rare:14 | ||||
| chr7:93117948-93118123 | Rare:30 | ||||
| chr7:93232139-93232389 | Common:2; Rare:53 | ||||
| chr7:93890599-93890949 | Common:4; Rare:98 | ||||
| chr7:94004295-94004478 | Rare:51 | ||||
| chr7:94656118-94656381 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:96709772-96709923 | Rare:52 | ||||
| chr7:97117449-97117763 | Common:2; Rare:134 |