| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109691145-109691348 | Common:3; Rare:49; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179882-110180144 | Common:2; Rare:74 | ||||
| chr6:110815119-110815458 | Common:2; Rare:105 | ||||
| chr6:110815847-110815931 | Common:1; Rare:27 | ||||
| chr6:110874624-110874798 | Common:4; Rare:59 | ||||
| chr6:110958428-110958545 | Common:2; Rare:32 | ||||
| chr6:110958574-110958781 | Common:4; Rare:73 | ||||
| chr6:110981963-110982100 | Common:2; Rare:67 | ||||
| chr6:111259135-111259366 | Common:2; Rare:71 | ||||
| chr6:111483208-111483648 | Common:1; Rare:157 | ||||
| chr6:111573701-111573794 | Common:1; Rare:17 | ||||
| chr6:112087409-112087695 | Rare:91 | ||||
| chr6:113857247-113857430 | Common:1; Rare:44 | ||||
| chr6:113969662-113970164 | Common:1; Rare:105 | ||||
| chr6:113970695-113970861 | Rare:47 |