| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:72828175-72828502 | Rare:81 | ||||
| chr7:73557574-73557753 | Common:2; Rare:66 | ||||
| chr7:73683399-73683622 | Common:3; Rare:91 | ||||
| chr7:73738708-73739216 | Common:2; Rare:164 | ||||
| chr7:73770246-73770358 | Rare:21 | ||||
| chr7:73842506-73842716 | Common:6; Rare:32 | ||||
| chr7:74254385-74254528 | Rare:66 | ||||
| chr7:74289331-74289657 | Common:5; Rare:122 | ||||
| chr7:74657459-74657755 | Common:2; Rare:86 | ||||
| chr7:74657962-74658067 | Common:1; Rare:20 | ||||
| chr7:75914917-75915198 | Common:3; Rare:102; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:75980129-75980437 | Common:2; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75980880-75981144 | Rare:95; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:75981857-75982290 | Common:3; Rare:123; Clinvar:1 | ||||
| chr7:75983407-75983567 | Common:3; Rare:46; Clinvar (pathogenic):1 |