| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:133951884-133952081 | Common:3; Rare:38 | ||||
| chr6:133952342-133952469 | Rare:22 | ||||
| chr6:133952949-133953251 | Common:2; Rare:82 | ||||
| chr6:134052100-134052400 | Rare:59 | ||||
| chr6:134052642-134052785 | Common:1; Rare:22 | ||||
| chr6:134174851-134175118 | Common:1; Rare:120 | ||||
| chr6:134175566-134175778 | Rare:72 | ||||
| chr6:135054760-135055036 | Common:6; Rare:85 | ||||
| chr6:135181144-135181279 | Rare:39 | ||||
| chr6:135497705-135497935 | Common:3; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:136250263-136250578 | Common:2; Rare:94 | ||||
| chr6:136289252-136289457 | Rare:86 | ||||
| chr6:136289777-136290178 | Common:2; Rare:153 | ||||
| chr6:136822445-136822643 | Common:5; Rare:67; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:136822781-136822972 | Common:2; Rare:75; Clinvar:4; Clinvar (pathogenic):2 |