| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:107115236-107115345 | Rare:29 | ||||
| chr6:107115434-107115555 | Common:1; Rare:29 | ||||
| chr6:107459425-107459743 | Common:4; Rare:154; Clinvar:2 | ||||
| chr6:107489893-107490257 | Common:2; Rare:238 | ||||
| chr6:107490267-107490667 | Common:8; Rare:171 | ||||
| chr6:107957150-107957430 | Common:1; Rare:74 | ||||
| chr6:107958012-107958450 | Common:4; Rare:267; Clinvar:4; Clinvar (benign):6 | ||||
| chr6:108074661-108074936 | Common:2; Rare:170; Clinvar:2 | ||||
| chr6:108260907-108261402 | Common:4; Rare:388 | ||||
| chr6:108294801-108295087 | Common:2; Rare:149 | ||||
| chr6:108559458-108559844 | Common:8; Rare:266 | ||||
| chr6:108560726-108561009 | Rare:228 | ||||
| chr6:108848322-108848479 | Rare:60 | ||||
| chr6:109009430-109009725 | Common:4; Rare:144 | ||||
| chr6:109094818-109095200 | Common:9; Rare:225 |