| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:92134409-92134585 | Rare:57 | ||||
| chr7:92134731-92134852 | Common:3; Rare:28 | ||||
| chr7:92245668-92246305 | Common:6; Rare:156; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92447224-92447472 | Common:2; Rare:69 | ||||
| chr7:92528383-92528822 | Common:4; Rare:137; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92833902-92834089 | Rare:46 | ||||
| chr7:92836458-92836507 | Rare:10 | ||||
| chr7:93232201-93232417 | Common:2; Rare:44 | ||||
| chr7:93890756-93890835 | Common:1; Rare:22 | ||||
| chr7:93921612-93922139 | Common:7; Rare:117 | ||||
| chr7:94004295-94004520 | Rare:63 | ||||
| chr7:94425617-94425763 | Rare:50; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:94425766-94426060 | Rare:87; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:94509704-94510087 | Rare:129 | ||||
| chr7:94656063-94656387 | Common:2; Rare:85; Clinvar:4; Clinvar (benign):3 |