| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:82364221-82364307 | Common:1; Rare:24 | ||||
| chr6:83193222-83193414 | Common:3; Rare:70 | ||||
| chr6:84763442-84763614 | Rare:43 | ||||
| chr6:84764575-84764773 | Rare:56 | ||||
| chr6:85449553-85449733 | Common:1; Rare:44 | ||||
| chr6:85449927-85450150 | Common:1; Rare:68 | ||||
| chr6:85593693-85593975 | Common:1; Rare:97 | ||||
| chr6:85643796-85643923 | Common:3; Rare:40 | ||||
| chr6:85644154-85644417 | Rare:58 | ||||
| chr6:87155262-87155601 | Rare:89 | ||||
| chr6:87589953-87590160 | Common:2; Rare:91; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87701878-87702013 | Rare:44 | ||||
| chr6:88963506-88963824 | Common:2; Rare:97 | ||||
| chr6:89081049-89081387 | Common:2; Rare:129 | ||||
| chr6:89117962-89118091 | Common:1; Rare:52 |