| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:91940755-91941039 | Common:4; Rare:91; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:91941059-91941111 | Rare:16; Clinvar (benign):1 | ||||
| chr7:92134409-92134891 | Common:5; Rare:141 | ||||
| chr7:92245663-92245979 | Rare:76; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92246117-92246511 | Common:3; Rare:158 | ||||
| chr7:92528364-92528816 | Common:3; Rare:138; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92833665-92833752 | Rare:22 | ||||
| chr7:92836486-92836620 | Rare:28 | ||||
| chr7:93232294-93232440 | Common:3; Rare:36 | ||||
| chr7:94656109-94656380 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95396289-95396508 | Common:2; Rare:101 | ||||
| chr7:95592509-95592887 | Common:2; Rare:109 | ||||
| chr7:95596162-95596689 | Common:6; Rare:137 | ||||
| chr7:96321942-96322144 | Common:1; Rare:96; Clinvar:6 | ||||
| chr7:97024338-97024510 | Rare:58 |