| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:125956661-125956925 | Common:1; Rare:72 | ||||
| chr6:125986385-125986550 | Rare:55 | ||||
| chr6:125986630-125986698 | Rare:23 | ||||
| chr6:127266756-127266889 | Common:2; Rare:57 | ||||
| chr6:127342402-127342560 | Common:1; Rare:31 | ||||
| chr6:127343344-127343433 | Rare:16 | ||||
| chr6:127343527-127343645 | Common:1; Rare:34 | ||||
| chr6:128520474-128520798 | Common:3; Rare:106 | ||||
| chr6:129490595-129490726 | Common:1; Rare:22 | ||||
| chr6:129491074-129491229 | Rare:35 | ||||
| chr6:132798590-132798880 | Common:9; Rare:61 | ||||
| chr6:132814313-132814612 | Common:3; Rare:114 | ||||
| chr6:133953025-133953241 | Common:2; Rare:63 | ||||
| chr6:134174847-134175047 | Common:1; Rare:98 | ||||
| chr6:135497728-135497873 | Common:3; Rare:52; Clinvar:1; Clinvar (benign):1 |