| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79537364-79537648 | Common:2; Rare:86; Clinvar:4 | ||||
| chr6:80004375-80004687 | Common:6; Rare:77 | ||||
| chr6:83193201-83193389 | Common:3; Rare:62 | ||||
| chr6:85449943-85450133 | Common:1; Rare:56 | ||||
| chr6:85593781-85593987 | Common:1; Rare:67 | ||||
| chr6:85642848-85643081 | Common:3; Rare:82 | ||||
| chr6:85643796-85643931 | Common:3; Rare:43 | ||||
| chr6:87155263-87155588 | Rare:86 | ||||
| chr6:87589953-87590169 | Common:3; Rare:98; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:89117950-89118122 | Common:3; Rare:77 | ||||
| chr6:89638450-89638537 | Common:1; Rare:19 | ||||
| chr6:89638712-89638835 | Common:3; Rare:45 | ||||
| chr6:89829619-89829955 | Rare:88 | ||||
| chr6:90586976-90587334 | Common:3; Rare:97 | ||||
| chr6:95577408-95577571 | Common:4; Rare:45 |