| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:92246058-92246519 | Common:3; Rare:167; Clinvar:1 | ||||
| chr7:92447226-92447472 | Common:2; Rare:68 | ||||
| chr7:92528313-92528816 | Common:3; Rare:151; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92836333-92836518 | Rare:39 | ||||
| chr7:93232201-93232417 | Common:2; Rare:44 | ||||
| chr7:93574716-93574947 | Common:1; Rare:53 | ||||
| chr7:93890747-93890868 | Common:2; Rare:31 | ||||
| chr7:94394537-94394937 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:94425766-94426050 | Rare:87; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:94656053-94656473 | Common:2; Rare:88; Clinvar:4; Clinvar (benign):3 | ||||
| chr7:94908433-94908514 | Rare:14 | ||||
| chr7:95434893-95435097 | Common:1; Rare:89; Clinvar (benign):1 | ||||
| chr7:95596512-95596713 | Common:2; Rare:39 | ||||
| chr7:97117475-97117804 | Common:1; Rare:146 | ||||
| chr7:98252145-98252378 | Common:1; Rare:56 |