| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:86643712-86643922 | Rare:44 | ||||
| chr7:87152329-87152474 | Common:1; Rare:50 | ||||
| chr7:87345470-87345701 | Common:4; Rare:75 | ||||
| chr7:87628250-87628499 | Rare:73 | ||||
| chr7:87876276-87876652 | Common:2; Rare:169 | ||||
| chr7:88220024-88220174 | Rare:68 | ||||
| chr7:90245083-90245185 | Rare:30 | ||||
| chr7:90346586-90346736 | Common:3; Rare:62 | ||||
| chr7:91880656-91880834 | Common:2; Rare:49 | ||||
| chr7:91940808-91941040 | Common:4; Rare:77; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134409-92134550 | Rare:39 | ||||
| chr7:92134709-92134890 | Common:3; Rare:54 | ||||
| chr7:92245865-92245974 | Rare:33; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92246105-92246473 | Common:3; Rare:138 | ||||
| chr7:92528370-92528816 | Common:3; Rare:137; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 |