| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:80004382-80004654 | Common:5; Rare:67 | ||||
| chr6:81752660-81752863 | Rare:102 | ||||
| chr6:83193222-83193389 | Common:3; Rare:58 | ||||
| chr6:85449531-85449732 | Common:1; Rare:50 | ||||
| chr6:85449909-85450140 | Common:1; Rare:69 | ||||
| chr6:85593804-85593975 | Rare:56 | ||||
| chr6:85643817-85643931 | Common:2; Rare:36 | ||||
| chr6:87155248-87155717 | Rare:141 | ||||
| chr6:87589946-87590160 | Common:2; Rare:97; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:87702199-87702443 | Common:1; Rare:79 | ||||
| chr6:88963569-88963818 | Common:2; Rare:83 | ||||
| chr6:89080571-89080800 | Common:1; Rare:98 | ||||
| chr6:89081022-89081427 | Common:2; Rare:156 | ||||
| chr6:89145983-89146090 | Rare:32 | ||||
| chr6:89638438-89638596 | Common:1; Rare:31 |