| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66371546-66371636 | Rare:22 | ||||
| chr7:66493507-66493751 | Common:4; Rare:101 | ||||
| chr7:66592272-66592474 | Common:2; Rare:73 | ||||
| chr7:66654444-66654602 | Rare:63 | ||||
| chr7:66844858-66845127 | Common:2; Rare:114 | ||||
| chr7:66991154-66991558 | Rare:89; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr7:67302394-67302814 | Common:5; Rare:129 | ||||
| chr7:72954695-72954824 | Common:1; Rare:22 | ||||
| chr7:73003024-73003110 | Rare:14 | ||||
| chr7:73005518-73005584 | Rare:5 | ||||
| chr7:73005765-73006164 | Common:1; Rare:45 | ||||
| chr7:74043320-74043346 | Rare:5 | ||||
| chr7:74043592-74043905 | Rare:58; Clinvar (pathogenic):1 | ||||
| chr7:74058397-74058421 | Rare:1 | ||||
| chr7:74059682-74060047 | Common:2; Rare:126; Clinvar:1; Clinvar (benign):4 |