| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79234550-79234775 | Common:2; Rare:57 | ||||
| chr6:79537383-79537633 | Common:1; Rare:71; Clinvar:3 | ||||
| chr6:79631224-79631464 | Rare:72 | ||||
| chr6:80004390-80004674 | Common:6; Rare:70 | ||||
| chr6:81752657-81752842 | Rare:93 | ||||
| chr6:83193194-83193403 | Common:3; Rare:70 | ||||
| chr6:84227604-84227731 | Rare:35 | ||||
| chr6:85449933-85450150 | Common:1; Rare:65 | ||||
| chr6:85593800-85594104 | Common:1; Rare:87 | ||||
| chr6:85643812-85643946 | Common:2; Rare:41 | ||||
| chr6:87155226-87155614 | Rare:107 | ||||
| chr6:87472900-87473006 | Common:1; Rare:41; Clinvar (benign):4 | ||||
| chr6:87589955-87590165 | Common:2; Rare:93; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87702223-87702476 | Common:1; Rare:75 | ||||
| chr6:88963540-88963862 | Common:2; Rare:111 |