| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79631156-79631374 | Common:2; Rare:55 | ||||
| chr6:80004392-80004640 | Common:5; Rare:60 | ||||
| chr6:81752668-81752837 | Rare:87 | ||||
| chr6:82364213-82364281 | Common:1; Rare:18 | ||||
| chr6:83068022-83068147 | Common:1; Rare:27 | ||||
| chr6:83193222-83193389 | Common:3; Rare:58 | ||||
| chr6:84764577-84764758 | Rare:55 | ||||
| chr6:85449905-85450144 | Common:1; Rare:71 | ||||
| chr6:85593722-85593923 | Common:1; Rare:73 | ||||
| chr6:85643296-85643615 | Common:1; Rare:112 | ||||
| chr6:85643812-85643874 | Rare:23 | ||||
| chr6:87155267-87155615 | Rare:98 | ||||
| chr6:87472900-87473006 | Common:1; Rare:41; Clinvar (benign):4 | ||||
| chr6:87589955-87590165 | Common:2; Rare:93; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87702224-87702445 | Common:1; Rare:65 |