| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:76302496-76302710 | Common:2; Rare:78; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:76302818-76303075 | Rare:113; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr7:77122360-77122671 | Common:1; Rare:64 | ||||
| chr7:77328259-77328377 | Common:3; Rare:17 | ||||
| chr7:77416355-77416449 | Common:1; Rare:21 | ||||
| chr7:77696133-77696497 | Common:1; Rare:145 | ||||
| chr7:77697050-77697204 | Common:2; Rare:44 | ||||
| chr7:77798324-77798956 | Common:1; Rare:151 | ||||
| chr7:79452783-79453191 | Common:2; Rare:99; Clinvar (benign):2 | ||||
| chr7:79453549-79453772 | Common:1; Rare:56 | ||||
| chr7:79453776-79454117 | Common:2; Rare:82 | ||||
| chr7:80134497-80134935 | Common:4; Rare:139 | ||||
| chr7:80623955-80624138 | Common:1; Rare:34 | ||||
| chr7:80918981-80919287 | Common:3; Rare:96 | ||||
| chr7:82443448-82443881 | Common:3; Rare:142; Clinvar (benign):1 |