| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:93232194-93232387 | Common:2; Rare:37 | ||||
| chr7:93890589-93890834 | Common:3; Rare:80 | ||||
| chr7:93921635-93922182 | Common:7; Rare:127 | ||||
| chr7:94004303-94004462 | Rare:47 | ||||
| chr7:94394672-94395038 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:94425775-94426043 | Rare:82; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:94656105-94656374 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:97117503-97117774 | Common:1; Rare:117 | ||||
| chr7:98252170-98252372 | Common:1; Rare:48 | ||||
| chr7:99325801-99325997 | Common:1; Rare:77 | ||||
| chr7:99408549-99408779 | Common:2; Rare:58 | ||||
| chr7:99408782-99409053 | Common:1; Rare:83 | ||||
| chr7:99438715-99438996 | Common:1; Rare:94 | ||||
| chr7:99466120-99466242 | Rare:48 | ||||
| chr7:99472635-99472912 | Common:4; Rare:86 |