| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44796503-44796722 | Common:2; Rare:95 | ||||
| chr7:45111687-45111806 | Common:1; Rare:41 | ||||
| chr7:47539594-47539837 | Common:2; Rare:47 | ||||
| chr7:56034118-56034277 | Rare:47 | ||||
| chr7:56051439-56051865 | Common:1; Rare:164; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56106418-56106713 | Common:8; Rare:100 | ||||
| chr7:66114637-66114908 | Common:4; Rare:89 | ||||
| chr7:66115186-66115354 | Rare:38 | ||||
| chr7:66205093-66205355 | Rare:66 | ||||
| chr7:73683419-73683622 | Common:3; Rare:81 | ||||
| chr7:73738786-73739146 | Common:2; Rare:114 | ||||
| chr7:73842505-73842682 | Common:6; Rare:24 | ||||
| chr7:74174114-74174412 | Common:1; Rare:155 | ||||
| chr7:74254366-74254528 | Rare:75 | ||||
| chr7:75914911-75915168 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):1 |