| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:92246116-92246482 | Common:3; Rare:143 | ||||
| chr7:92528370-92528816 | Common:3; Rare:137; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590040-92590123 | Rare:34 | ||||
| chr7:92833902-92834096 | Rare:47 | ||||
| chr7:93117904-93118123 | Rare:34 | ||||
| chr7:93219554-93219703 | Rare:15 | ||||
| chr7:93232201-93232431 | Common:3; Rare:49 | ||||
| chr7:93890743-93890944 | Common:2; Rare:45 | ||||
| chr7:93921925-93922129 | Common:4; Rare:50 | ||||
| chr7:94004262-94004522 | Rare:70 | ||||
| chr7:94656053-94656491 | Common:2; Rare:88; Clinvar:4; Clinvar (benign):3 | ||||
| chr7:95396276-95396678 | Common:3; Rare:136 | ||||
| chr7:95434884-95435147 | Common:1; Rare:112; Clinvar (benign):1 | ||||
| chr7:95596507-95596718 | Common:2; Rare:40 | ||||
| chr7:96321942-96322327 | Common:1; Rare:142; Clinvar:6 |