| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42929232-42929549 | Common:3; Rare:85 | ||||
| chr6:43013886-43014297 | Common:2; Rare:91 | ||||
| chr6:43059818-43059913 | Rare:31 | ||||
| chr6:43516852-43517115 | Common:5; Rare:97; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575957-43576147 | Rare:72 | ||||
| chr6:44127359-44127629 | Common:4; Rare:76 | ||||
| chr6:46652760-46652975 | Rare:58 | ||||
| chr6:49463194-49463430 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52576889-52577292 | Common:6; Rare:145 | ||||
| chr6:56843630-56843928 | Common:9; Rare:66 | ||||
| chr6:57046502-57046708 | Rare:64 | ||||
| chr6:57089929-57090192 | Rare:97 | ||||
| chr6:57317547-57317652 | Rare:30 | ||||
| chr6:73263165-73263279 | Common:2; Rare:29 | ||||
| chr6:73696150-73696235 | Rare:28 |