| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74174104-74174439 | Common:1; Rare:160 | ||||
| chr7:74254309-74254575 | Rare:125 | ||||
| chr7:74453096-74453319 | Common:1; Rare:46 | ||||
| chr7:74453887-74454150 | Common:1; Rare:76 | ||||
| chr7:74505395-74505582 | Rare:36 | ||||
| chr7:74657448-74657724 | Common:2; Rare:85 | ||||
| chr7:75093050-75093233 | Rare:22 | ||||
| chr7:75878853-75879085 | Common:12; Rare:86 | ||||
| chr7:75914957-75915168 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994502-75994791 | Common:4; Rare:144 | ||||
| chr7:76047950-76048194 | Common:2; Rare:83 | ||||
| chr7:76302462-76302673 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:76302875-76302983 | Rare:53; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr7:76303536-76303817 | Common:2; Rare:123; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:76358919-76359088 | Rare:76 |