| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:87345176-87345219 | Rare:6 | ||||
| chr7:87345222-87345762 | Common:7; Rare:151 | ||||
| chr7:87876204-87876657 | Common:2; Rare:192 | ||||
| chr7:90595933-90596009 | Common:5; Rare:27 | ||||
| chr7:91880638-91880801 | Common:1; Rare:46 | ||||
| chr7:92134381-92134567 | Rare:60 | ||||
| chr7:92134717-92135038 | Common:3; Rare:81 | ||||
| chr7:92245836-92246274 | Common:6; Rare:110; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92528438-92528870 | Common:5; Rare:143; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:93921667-93922153 | Common:7; Rare:113 | ||||
| chr7:94394532-94395082 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:94413888-94414275 | Common:3; Rare:88; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:94419456-94419551 | Common:2; Rare:18; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:94421888-94422181 | Common:2; Rare:53; Clinvar (benign):1 | ||||
| chr7:94422951-94423279 | Common:1; Rare:81; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 |