| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:57046494-57046729 | Rare:80 | ||||
| chr6:57172352-57172764 | Common:1; Rare:122 | ||||
| chr6:63572190-63572610 | Rare:154 | ||||
| chr6:63635676-63635886 | Rare:88 | ||||
| chr6:69796867-69797112 | Rare:79; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:70413188-70413595 | Common:2; Rare:120 | ||||
| chr6:73263153-73263279 | Common:3; Rare:34 | ||||
| chr6:73394622-73394900 | Common:4; Rare:88 | ||||
| chr6:73653934-73654174 | Common:3; Rare:66; Clinvar:3 | ||||
| chr6:73696030-73696207 | Rare:35 | ||||
| chr6:75243710-75243972 | Common:1; Rare:119 | ||||
| chr6:75284722-75285033 | Common:1; Rare:89 | ||||
| chr6:75493777-75493899 | Common:1; Rare:27 | ||||
| chr6:75601789-75601952 | Rare:60 | ||||
| chr6:75602279-75602527 | Common:1; Rare:72 |