| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:10404160-10404512 | Common:3; Rare:152; Clinvar (pathogenic):1 | ||||
| chr6:10491960-10492230 | Common:6; Rare:91 | ||||
| chr6:10694541-10695019 | Common:8; Rare:151 | ||||
| chr6:10722902-10723240 | Common:5; Rare:125 | ||||
| chr6:10747597-10747865 | Common:3; Rare:105 | ||||
| chr6:10838444-10838663 | Common:4; Rare:57; Clinvar:4 | ||||
| chr6:10886714-10887071 | Common:7; Rare:104 | ||||
| chr6:11044228-11044711 | Common:4; Rare:151 | ||||
| chr6:11093644-11093831 | Rare:60 | ||||
| chr6:11232563-11232625 | Rare:20 | ||||
| chr6:11232627-11232686 | Rare:13 | ||||
| chr6:11779609-11779695 | Rare:12 | ||||
| chr6:13328474-13328652 | Common:5; Rare:72 | ||||
| chr6:13615170-13615629 | Common:2; Rare:182 | ||||
| chr6:13924809-13925012 | Common:1; Rare:76 |