| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:93890731-93890942 | Common:2; Rare:49 | ||||
| chr7:93921926-93922167 | Common:4; Rare:68 | ||||
| chr7:94004297-94004558 | Rare:70 | ||||
| chr7:94394521-94395326 | Common:1; Rare:168; Clinvar:2; Clinvar (benign):4 | ||||
| chr7:94414175-94414438 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:94417684-94417869 | Common:1; Rare:46; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:94425748-94425933 | Rare:59; Clinvar:4; Clinvar (benign):3 | ||||
| chr7:94425990-94426373 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:94426902-94427304 | Common:4; Rare:101; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:94656053-94656422 | Common:2; Rare:88; Clinvar:4; Clinvar (benign):3 | ||||
| chr7:94908422-94908507 | Rare:12 | ||||
| chr7:95596507-95596718 | Common:2; Rare:40 | ||||
| chr7:97872425-97872548 | Rare:37 | ||||
| chr7:98252165-98252372 | Common:1; Rare:49 | ||||
| chr7:98878397-98878621 | Rare:79 |