| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:93921630-93922182 | Common:7; Rare:128 | ||||
| chr7:94004262-94004506 | Rare:65 | ||||
| chr7:94656070-94656411 | Common:2; Rare:80; Clinvar:4; Clinvar (benign):3 | ||||
| chr7:95434884-95435097 | Common:1; Rare:90; Clinvar (benign):1 | ||||
| chr7:95596135-95596237 | Rare:43 | ||||
| chr7:95596278-95596438 | Common:1; Rare:45 | ||||
| chr7:95596489-95596731 | Common:4; Rare:44 | ||||
| chr7:95596897-95596926 | Rare:6 | ||||
| chr7:96321963-96322273 | Rare:126; Clinvar:4 | ||||
| chr7:96709745-96709923 | Common:1; Rare:57 | ||||
| chr7:97006390-97006472 | Common:1; Rare:23 | ||||
| chr7:97117448-97117813 | Common:2; Rare:162 | ||||
| chr7:97871512-97871544 | Rare:9 | ||||
| chr7:97872205-97872583 | Common:6; Rare:127 | ||||
| chr7:98252165-98252378 | Common:1; Rare:51 |