| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79077710-79077935 | Common:1; Rare:62 | ||||
| chr6:79078160-79078608 | Common:1; Rare:190 | ||||
| chr6:79537373-79537643 | Common:1; Rare:78; Clinvar:3 | ||||
| chr6:80004503-80004674 | Common:3; Rare:39 | ||||
| chr6:80106450-80106690 | Common:1; Rare:77 | ||||
| chr6:82247742-82247828 | Rare:26 | ||||
| chr6:83065743-83065987 | Common:1; Rare:79 | ||||
| chr6:83067416-83067776 | Common:1; Rare:89 | ||||
| chr6:83193194-83193403 | Common:3; Rare:70 | ||||
| chr6:83859546-83859724 | Rare:62 | ||||
| chr6:85593783-85594107 | Common:2; Rare:92 | ||||
| chr6:87155243-87155631 | Rare:111 | ||||
| chr6:87472900-87473006 | Common:1; Rare:41; Clinvar (benign):4 | ||||
| chr6:87589946-87590171 | Common:3; Rare:106; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:87702189-87702531 | Common:2; Rare:108 |