| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:85449939-85450135 | Common:1; Rare:57 | ||||
| chr6:85593714-85594007 | Common:1; Rare:95 | ||||
| chr6:85643302-85643365 | Rare:30 | ||||
| chr6:85643817-85643931 | Common:2; Rare:36 | ||||
| chr6:87155240-87155594 | Rare:94 | ||||
| chr6:87472862-87472998 | Common:1; Rare:48; Clinvar (benign):4 | ||||
| chr6:87589955-87590165 | Common:2; Rare:93; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87702189-87702514 | Common:2; Rare:102 | ||||
| chr6:88963579-88963830 | Common:2; Rare:84 | ||||
| chr6:89081029-89081350 | Common:2; Rare:126 | ||||
| chr6:89081629-89081813 | Common:2; Rare:57 | ||||
| chr6:89117950-89118103 | Common:2; Rare:69 | ||||
| chr6:89145941-89146090 | Rare:41 | ||||
| chr6:89638438-89638806 | Common:6; Rare:111 | ||||
| chr6:89829603-89829955 | Rare:90 |