| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:40134588-40134940 | Rare:105 | ||||
| chr7:42932151-42932413 | Rare:105 | ||||
| chr7:43926389-43926457 | Rare:24 | ||||
| chr7:44044582-44044738 | Common:2; Rare:43 | ||||
| chr7:44573896-44574053 | Common:3; Rare:42 | ||||
| chr7:44582202-44582474 | Common:1; Rare:97 | ||||
| chr7:44606465-44606631 | Common:1; Rare:59 | ||||
| chr7:44796389-44796784 | Common:3; Rare:153 | ||||
| chr7:45111665-45111793 | Common:1; Rare:50 | ||||
| chr7:56051439-56051851 | Common:1; Rare:159; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:66114571-66114895 | Common:4; Rare:98 | ||||
| chr7:73683429-73683622 | Common:3; Rare:77 | ||||
| chr7:74174045-74174405 | Common:1; Rare:169 | ||||
| chr7:74254376-74254520 | Rare:64 | ||||
| chr7:76047980-76048191 | Common:2; Rare:66 |