| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:78867471-78867585 | Rare:47 | ||||
| chr6:79078028-79078598 | Common:1; Rare:227 | ||||
| chr6:79234593-79234729 | Common:1; Rare:39 | ||||
| chr6:79537346-79537650 | Common:2; Rare:92; Clinvar:4 | ||||
| chr6:79631233-79631387 | Rare:41 | ||||
| chr6:81752660-81752847 | Rare:96 | ||||
| chr6:83193222-83193391 | Common:3; Rare:59 | ||||
| chr6:85449912-85450344 | Common:1; Rare:128 | ||||
| chr6:85593706-85593932 | Common:1; Rare:84 | ||||
| chr6:85643822-85643931 | Common:2; Rare:34 | ||||
| chr6:87155262-87155601 | Rare:89 | ||||
| chr6:87472900-87472996 | Common:1; Rare:38; Clinvar (benign):4 | ||||
| chr6:87589920-87590163 | Common:2; Rare:121; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr6:88963506-88963773 | Rare:81 | ||||
| chr6:89080467-89080880 | Common:3; Rare:157 |