| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:47470648-47470872 | Rare:47 | ||||
| chr7:50641416-50641688 | Common:1; Rare:49 | ||||
| chr7:55188932-55189142 | Common:2; Rare:47 | ||||
| chr7:55688327-55688490 | Rare:26 | ||||
| chr7:65065823-65065996 | Common:1; Rare:36 | ||||
| chr7:65081199-65081428 | Common:3; Rare:77 | ||||
| chr7:65731758-65731883 | Common:1; Rare:25 | ||||
| chr7:65750287-65750477 | Common:3; Rare:40 | ||||
| chr7:65750910-65751144 | Common:4; Rare:102 | ||||
| chr7:65755365-65755528 | Common:1; Rare:41 | ||||
| chr7:65762708-65762981 | Common:2; Rare:25 | ||||
| chr7:65770719-65770940 | Common:6; Rare:71 | ||||
| chr7:65964323-65964690 | Common:2; Rare:93; Clinvar (benign):2 | ||||
| chr7:66081617-66081937 | Rare:68; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:66292885-66292906 | Rare:2 |