| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:64903119-64903298 | Common:2; Rare:45 | ||||
| chr7:65006638-65006864 | Common:2; Rare:68 | ||||
| chr7:66114756-66114904 | Common:1; Rare:71 | ||||
| chr7:66115177-66115374 | Common:1; Rare:45 | ||||
| chr7:66681974-66682167 | Common:5; Rare:85 | ||||
| chr7:66996557-66996872 | Common:2; Rare:73 | ||||
| chr7:73308786-73308897 | Rare:41 | ||||
| chr7:73683429-73683659 | Common:3; Rare:104 | ||||
| chr7:73738798-73739017 | Common:1; Rare:64 | ||||
| chr7:74254363-74254535 | Rare:81 | ||||
| chr7:75878848-75879076 | Common:12; Rare:83 | ||||
| chr7:75914964-75915164 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994512-75994741 | Common:3; Rare:113 | ||||
| chr7:76047964-76048191 | Common:2; Rare:72 | ||||
| chr7:76302862-76303075 | Rare:89; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 |