| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:91880667-91880791 | Common:1; Rare:33 | ||||
| chr7:91940761-91941048 | Common:4; Rare:90; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134351-92134550 | Rare:54 | ||||
| chr7:92134693-92134891 | Common:4; Rare:59 | ||||
| chr7:92245849-92245974 | Rare:35; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92246099-92246493 | Common:3; Rare:151 | ||||
| chr7:92528358-92528816 | Common:3; Rare:139; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590311-92590483 | Common:1; Rare:65 | ||||
| chr7:92833906-92834007 | Rare:28 | ||||
| chr7:93148359-93148389 | Rare:5 | ||||
| chr7:93148390-93148631 | Common:1; Rare:35 | ||||
| chr7:93232127-93232417 | Common:2; Rare:67 | ||||
| chr7:94004303-94004506 | Rare:57 | ||||
| chr7:94394690-94395099 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:94656053-94656562 | Common:2; Rare:88; Clinvar:4; Clinvar (benign):3 |