| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:87345476-87345701 | Common:4; Rare:71 | ||||
| chr7:87709415-87709457 | Rare:10 | ||||
| chr7:87876208-87876634 | Common:2; Rare:179 | ||||
| chr7:90211633-90211913 | Common:4; Rare:86 | ||||
| chr7:90346491-90346733 | Common:3; Rare:92 | ||||
| chr7:90595880-90596018 | Common:6; Rare:49 | ||||
| chr7:91880677-91880822 | Common:2; Rare:38 | ||||
| chr7:91940812-91940995 | Common:4; Rare:62; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134400-92134599 | Rare:64 | ||||
| chr7:92134779-92134880 | Common:2; Rare:33 | ||||
| chr7:92245843-92245986 | Rare:38; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528394-92528808 | Common:3; Rare:129; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:93232201-93232389 | Common:2; Rare:34 | ||||
| chr7:94656118-94656370 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95587008-95587530 | Common:7; Rare:155 |