| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:80004509-80004702 | Common:3; Rare:41 | ||||
| chr6:81752668-81752863 | Rare:98 | ||||
| chr6:83193194-83193429 | Common:3; Rare:79 | ||||
| chr6:84227587-84227964 | Common:4; Rare:88 | ||||
| chr6:85449880-85450144 | Common:1; Rare:77 | ||||
| chr6:85593714-85593930 | Common:1; Rare:77 | ||||
| chr6:85593949-85594044 | Rare:24 | ||||
| chr6:85643812-85643954 | Common:2; Rare:42 | ||||
| chr6:87155248-87155615 | Rare:100 | ||||
| chr6:87472900-87473004 | Common:1; Rare:40; Clinvar (benign):4 | ||||
| chr6:87589899-87590192 | Common:3; Rare:155; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr6:87702189-87702435 | Common:2; Rare:80 | ||||
| chr6:88963555-88963830 | Common:2; Rare:93 | ||||
| chr6:89080578-89080805 | Common:1; Rare:101 | ||||
| chr6:89081512-89081841 | Common:4; Rare:112 |