| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:84763455-84763541 | Rare:24 | ||||
| chr6:85449531-85449732 | Common:1; Rare:50 | ||||
| chr6:85449905-85450142 | Common:1; Rare:70 | ||||
| chr6:85593720-85594064 | Common:2; Rare:113 | ||||
| chr6:85643808-85643931 | Common:2; Rare:37 | ||||
| chr6:87155240-87155615 | Rare:104 | ||||
| chr6:87472802-87473005 | Common:1; Rare:63; Clinvar (benign):4 | ||||
| chr6:87589955-87590186 | Common:3; Rare:108; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87701832-87702013 | Common:1; Rare:61 | ||||
| chr6:87702215-87702534 | Common:1; Rare:98 | ||||
| chr6:88165868-88166018 | Rare:49 | ||||
| chr6:88963555-88963649 | Rare:25 | ||||
| chr6:89080581-89080824 | Common:1; Rare:105 | ||||
| chr6:89081022-89081381 | Common:2; Rare:140 | ||||
| chr6:89117950-89118093 | Common:1; Rare:57 |