| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:114084700-114084705 | Rare:1 | ||||
| chr6:116252774-116253228 | Common:1; Rare:149 | ||||
| chr6:116253529-116253634 | Rare:31 | ||||
| chr6:116277283-116277369 | Common:1; Rare:13 | ||||
| chr6:116277770-116277934 | Common:1; Rare:26 | ||||
| chr6:116431106-116431425 | Common:1; Rare:67; Clinvar (benign):2 | ||||
| chr6:116433202-116433546 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:116574126-116574233 | Rare:11 | ||||
| chr6:117546581-117546683 | Common:1; Rare:20 | ||||
| chr6:117570456-117570713 | Common:1; Rare:38 | ||||
| chr6:117599838-117600079 | Common:1; Rare:34 | ||||
| chr6:121437424-121437578 | Common:3; Rare:30 | ||||
| chr6:122437936-122438062 | Rare:25 | ||||
| chr6:122457948-122458039 | Common:1; Rare:15 | ||||
| chr6:122799786-122800063 | Common:2; Rare:41 |