| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79537153-79537227 | Rare:18; Clinvar:1 | ||||
| chr6:79537309-79537688 | Common:2; Rare:123; Clinvar:5 | ||||
| chr6:79631154-79631352 | Common:2; Rare:50 | ||||
| chr6:81752644-81752821 | Rare:93 | ||||
| chr6:83193221-83193407 | Common:3; Rare:67 | ||||
| chr6:85449521-85449743 | Common:1; Rare:57 | ||||
| chr6:85449993-85450144 | Common:1; Rare:47 | ||||
| chr6:85593804-85593909 | Rare:37 | ||||
| chr6:85643817-85643931 | Common:2; Rare:36 | ||||
| chr6:87155243-87155615 | Rare:102 | ||||
| chr6:87589955-87590165 | Common:2; Rare:93; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87701857-87701980 | Common:1; Rare:36 | ||||
| chr6:87702203-87702526 | Common:1; Rare:102 | ||||
| chr6:88963569-88963830 | Common:2; Rare:87 | ||||
| chr6:89081048-89081381 | Common:2; Rare:129 |