| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44986585-44986758 | Common:2; Rare:87 | ||||
| chr7:45768930-45769079 | Rare:41 | ||||
| chr7:64947587-64947827 | Common:3; Rare:68 | ||||
| chr7:64948981-64949138 | Common:1; Rare:36 | ||||
| chr7:65750916-65751080 | Common:2; Rare:66 | ||||
| chr7:66493534-66493729 | Common:3; Rare:84 | ||||
| chr7:66654231-66654568 | Common:2; Rare:112 | ||||
| chr7:66844870-66845011 | Rare:49 | ||||
| chr7:67302400-67302696 | Common:5; Rare:96 | ||||
| chr7:73005886-73006140 | Rare:22 | ||||
| chr7:74890542-74890812 | Common:2; Rare:81 | ||||
| chr7:85770614-85770681 | Rare:9 | ||||
| chr7:85773390-85773695 | Rare:56 | ||||
| chr7:92832894-92833146 | Common:1; Rare:52 | ||||
| chr7:94404553-94404746 | Rare:46; Clinvar:4; Clinvar (pathogenic):1 |