| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:80918870-80919174 | Rare:89 | ||||
| chr7:87152280-87152464 | Common:1; Rare:61 | ||||
| chr7:87345412-87345701 | Common:4; Rare:90 | ||||
| chr7:87876224-87876657 | Common:2; Rare:186 | ||||
| chr7:88219997-88220118 | Rare:65 | ||||
| chr7:90211644-90211886 | Common:3; Rare:75 | ||||
| chr7:90346564-90346736 | Common:3; Rare:72 | ||||
| chr7:90403312-90403512 | Common:1; Rare:50 | ||||
| chr7:90596243-90596479 | Rare:79 | ||||
| chr7:91880668-91880813 | Common:1; Rare:40 | ||||
| chr7:91940758-91940977 | Common:4; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:92134347-92134589 | Rare:75 | ||||
| chr7:92134683-92134891 | Common:4; Rare:61 | ||||
| chr7:92245865-92245974 | Rare:33; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528415-92528816 | Common:3; Rare:128; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 |