| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:92134400-92134558 | Rare:46 | ||||
| chr7:92134717-92134871 | Common:3; Rare:45 | ||||
| chr7:92245890-92245979 | Rare:27; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528385-92528893 | Common:5; Rare:164; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590310-92590420 | Common:1; Rare:47 | ||||
| chr7:93232180-93232405 | Common:2; Rare:48 | ||||
| chr7:94004284-94004462 | Rare:49 | ||||
| chr7:94656118-94656391 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95318037-95318360 | Common:1; Rare:60 | ||||
| chr7:95396268-95396623 | Common:3; Rare:129 | ||||
| chr7:95434879-95435227 | Common:1; Rare:132; Clinvar (benign):1 | ||||
| chr7:95596162-95596231 | Rare:27 | ||||
| chr7:95596283-95596347 | Rare:26 | ||||
| chr7:95596361-95596718 | Common:6; Rare:65 | ||||
| chr7:96121683-96121971 | Common:1; Rare:96; Clinvar:11; Clinvar (benign):2; Clinvar (pathogenic):4 |