| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:91940765-91941040 | Common:4; Rare:88; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134360-92134585 | Rare:71 | ||||
| chr7:92134744-92134823 | Common:2; Rare:18 | ||||
| chr7:92245828-92246482 | Common:6; Rare:208; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92528370-92528813 | Common:3; Rare:136; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590047-92590123 | Rare:31 | ||||
| chr7:93232189-93232395 | Common:2; Rare:39 | ||||
| chr7:93921962-93922182 | Common:4; Rare:63 | ||||
| chr7:94394591-94394959 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:94425779-94426050 | Rare:84; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:94656087-94656374 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:95396363-95396472 | Common:2; Rare:43 | ||||
| chr7:95587118-95587533 | Common:3; Rare:112 | ||||
| chr7:95589389-95589677 | Common:2; Rare:47 | ||||
| chr7:95592509-95592944 | Common:2; Rare:127 |