| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:84194550-84194912 | Common:3; Rare:58 | ||||
| chr7:87152270-87152562 | Common:2; Rare:91 | ||||
| chr7:87152565-87152795 | Rare:70 | ||||
| chr7:87345432-87345744 | Common:6; Rare:93 | ||||
| chr7:87876219-87876722 | Common:3; Rare:213 | ||||
| chr7:90245089-90245243 | Rare:52 | ||||
| chr7:90346573-90346752 | Common:4; Rare:80 | ||||
| chr7:90595840-90596046 | Common:6; Rare:76 | ||||
| chr7:91880656-91880927 | Common:2; Rare:78 | ||||
| chr7:91940727-91941041 | Common:5; Rare:98; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134360-92134605 | Rare:76 | ||||
| chr7:92134670-92134891 | Common:4; Rare:63 | ||||
| chr7:92245842-92246488 | Common:6; Rare:208; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92447312-92447505 | Common:3; Rare:65 | ||||
| chr7:92528306-92528838 | Common:4; Rare:166; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 |