| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:130366141-130366471 | Common:3; Rare:71 | ||||
| chr6:131250319-131250437 | Rare:21 | ||||
| chr6:131628101-131628416 | Common:3; Rare:88 | ||||
| chr6:132401428-132401596 | Common:1; Rare:51 | ||||
| chr6:132512712-132512833 | Common:2; Rare:38 | ||||
| chr6:133888891-133889140 | Common:2; Rare:47 | ||||
| chr6:133889323-133889604 | Common:4; Rare:95; Clinvar:1 | ||||
| chr6:133953047-133953246 | Common:2; Rare:62 | ||||
| chr6:134174622-134175059 | Common:1; Rare:212 | ||||
| chr6:134175685-134175741 | Rare:15 | ||||
| chr6:134177680-134178107 | Common:1; Rare:88 | ||||
| chr6:135054784-135055013 | Common:6; Rare:66 | ||||
| chr6:135497604-135497886 | Common:4; Rare:104; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289168-136289459 | Rare:105 | ||||
| chr6:136289756-136290024 | Common:1; Rare:116 |