| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:127342377-127342560 | Common:1; Rare:32 | ||||
| chr6:127343295-127343640 | Common:2; Rare:80 | ||||
| chr6:128520477-128520787 | Common:3; Rare:102 | ||||
| chr6:128882993-128883362 | Common:2; Rare:103; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr6:131628090-131628433 | Common:3; Rare:93 | ||||
| chr6:132401443-132401616 | Common:1; Rare:51 | ||||
| chr6:132513007-132513292 | Common:1; Rare:69 | ||||
| chr6:132757896-132758152 | Common:13; Rare:73 | ||||
| chr6:132814386-132814612 | Common:2; Rare:92 | ||||
| chr6:133953047-133953295 | Common:2; Rare:82 | ||||
| chr6:134174809-134175061 | Common:1; Rare:139 | ||||
| chr6:134175616-134175765 | Rare:53 | ||||
| chr6:135054792-135054962 | Common:5; Rare:49 | ||||
| chr6:135497603-135497860 | Common:4; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289756-136290054 | Common:2; Rare:128 |