| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:87152307-87152552 | Common:2; Rare:73 | ||||
| chr7:87345394-87345762 | Common:6; Rare:110 | ||||
| chr7:87876115-87876640 | Common:2; Rare:208 | ||||
| chr7:88219976-88220251 | Common:1; Rare:111 | ||||
| chr7:90211614-90211939 | Common:4; Rare:100 | ||||
| chr7:90346551-90346752 | Common:4; Rare:90 | ||||
| chr7:91880652-91880811 | Common:1; Rare:47 | ||||
| chr7:91940689-91941006 | Common:5; Rare:100; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:91941089-91941142 | Rare:17; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:92134159-92134373 | Rare:69 | ||||
| chr7:92245834-92246045 | Common:2; Rare:56; Clinvar:3; Clinvar (benign):4 | ||||
| chr7:92246046-92246274 | Common:4; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:92528428-92528877 | Common:5; Rare:151; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92833890-92833983 | Rare:26 | ||||
| chr7:93890307-93890606 | Common:3; Rare:91 |