| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:92245836-92246451 | Common:6; Rare:189; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92528370-92528816 | Common:3; Rare:137; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:93232301-93232385 | Common:2; Rare:16 | ||||
| chr7:93921775-93922182 | Common:5; Rare:102 | ||||
| chr7:94425766-94426043 | Rare:85; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:94656059-94656434 | Common:2; Rare:86; Clinvar:4; Clinvar (benign):3 | ||||
| chr7:94908385-94908436 | Rare:7 | ||||
| chr7:95396369-95396472 | Common:2; Rare:39 | ||||
| chr7:95596162-95596424 | Common:1; Rare:88 | ||||
| chr7:95596426-95596731 | Common:6; Rare:55 | ||||
| chr7:95596866-95596899 | Rare:2 | ||||
| chr7:97117462-97117787 | Common:2; Rare:145 | ||||
| chr7:98252143-98252402 | Common:2; Rare:64 | ||||
| chr7:98282089-98282446 | Common:2; Rare:126 | ||||
| chr7:99325801-99325979 | Common:1; Rare:69 |