| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:71131500-71131721 | Common:5; Rare:82 | ||||
| chr7:73308794-73308890 | Rare:34 | ||||
| chr7:73557113-73557370 | Common:1; Rare:91 | ||||
| chr7:73557606-73557767 | Common:2; Rare:54 | ||||
| chr7:73683413-73683624 | Common:3; Rare:85 | ||||
| chr7:73738786-73739146 | Common:2; Rare:114 | ||||
| chr7:73842478-73842682 | Common:6; Rare:35 | ||||
| chr7:74027995-74028140 | Rare:35; Clinvar:1 | ||||
| chr7:74174027-74174395 | Common:1; Rare:165 | ||||
| chr7:74254366-74254528 | Rare:75 | ||||
| chr7:74657456-74657724 | Common:2; Rare:80 | ||||
| chr7:75093050-75093199 | Rare:21 | ||||
| chr7:75842938-75843182 | Common:2; Rare:39 | ||||
| chr7:75878847-75879094 | Common:12; Rare:90 | ||||
| chr7:75914908-75915189 | Common:3; Rare:102; Clinvar:3; Clinvar (benign):1 |