| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:122471773-122471923 | Common:2; Rare:42 | ||||
| chr6:125956656-125956874 | Common:1; Rare:61 | ||||
| chr6:125986440-125986553 | Rare:44 | ||||
| chr6:127266767-127266916 | Common:2; Rare:65 | ||||
| chr6:127343331-127343431 | Rare:21 | ||||
| chr6:127343519-127343618 | Common:1; Rare:29 | ||||
| chr6:128520569-128520798 | Common:1; Rare:86 | ||||
| chr6:129710160-129710321 | Rare:41 | ||||
| chr6:131063145-131063474 | Rare:96 | ||||
| chr6:131628120-131628433 | Common:3; Rare:85 | ||||
| chr6:132814276-132814611 | Common:3; Rare:122 | ||||
| chr6:133241047-133241455 | Common:5; Rare:116 | ||||
| chr6:133952949-133953270 | Common:2; Rare:93 | ||||
| chr6:135054773-135055125 | Common:8; Rare:101; Clinvar:1 | ||||
| chr6:135497608-135497831 | Common:4; Rare:80; Clinvar:1; Clinvar (benign):2 |