| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:92836370-92836510 | Rare:27 | ||||
| chr7:93890727-93890949 | Common:2; Rare:53 | ||||
| chr7:93921797-93922172 | Common:5; Rare:96 | ||||
| chr7:94004187-94004484 | Rare:88 | ||||
| chr7:94394521-94394711 | Rare:33; Clinvar:1 | ||||
| chr7:94394721-94395102 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:94422035-94422198 | Common:2; Rare:24 | ||||
| chr7:94422960-94423702 | Common:7; Rare:158; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr7:94423715-94423912 | Rare:31 | ||||
| chr7:94424882-94425058 | Common:1; Rare:42 | ||||
| chr7:94425071-94425313 | Rare:64; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr7:94425479-94425663 | Rare:50; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:94425960-94426230 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:94656028-94656387 | Common:2; Rare:97; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:95434891-95435143 | Common:1; Rare:110; Clinvar (benign):1 |