| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166342492-166342657 | Common:3; Rare:67 | ||||
| chr6:166999021-166999433 | Common:2; Rare:142 | ||||
| chr6:169702000-169702196 | Common:3; Rare:100 | ||||
| chr6:169751534-169751645 | Rare:40; Clinvar (benign):1 | ||||
| chr6:170306559-170306808 | Common:1; Rare:82 | ||||
| chr6:170554197-170554445 | Common:2; Rare:78 | ||||
| chr7:519159-519294 | Rare:35 | ||||
| chr7:727223-727308 | Rare:29; Clinvar:1 | ||||
| chr7:975495-975650 | Common:1; Rare:74 | ||||
| chr7:1138196-1138451 | Common:2; Rare:81 | ||||
| chr7:1504332-1504511 | Common:3; Rare:83 | ||||
| chr7:1570007-1570151 | Common:1; Rare:47 | ||||
| chr7:1940139-1940327 | Common:2; Rare:42 | ||||
| chr7:2242168-2242274 | Common:2; Rare:61 | ||||
| chr7:2249157-2249325 | Common:3; Rare:35 |