| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:99349993-99350166 | Common:1; Rare:45 | ||||
| chr6:99424859-99424969 | Rare:41 | ||||
| chr6:99425214-99425506 | Common:2; Rare:86 | ||||
| chr6:99515395-99515580 | Common:1; Rare:63 | ||||
| chr6:100881068-100881482 | Common:7; Rare:134 | ||||
| chr6:104859557-104859635 | Common:1; Rare:13 | ||||
| chr6:104859736-104860010 | Common:1; Rare:82 | ||||
| chr6:104956772-104957194 | Rare:72 | ||||
| chr6:105402982-105403268 | Common:2; Rare:107 | ||||
| chr6:106325544-106325916 | Common:1; Rare:127 | ||||
| chr6:106629425-106629661 | Common:4; Rare:60 | ||||
| chr6:106975314-106975589 | Common:1; Rare:76 | ||||
| chr6:106975627-106975630 | |||||
| chr6:107028071-107028383 | Common:2; Rare:107 | ||||
| chr6:107458909-107459071 | Common:1; Rare:55; Clinvar:1; Clinvar (pathogenic):1 |