| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79078260-79078571 | Common:1; Rare:133 | ||||
| chr6:79234557-79234580 | Rare:6 | ||||
| chr6:79537346-79537658 | Common:2; Rare:98; Clinvar:4 | ||||
| chr6:79631173-79631385 | Common:2; Rare:51 | ||||
| chr6:83193236-83193407 | Common:3; Rare:61 | ||||
| chr6:85643817-85643881 | Rare:25 | ||||
| chr6:87155268-87155594 | Rare:87 | ||||
| chr6:87589940-87590171 | Common:3; Rare:111; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:88963569-88963830 | Common:2; Rare:87 | ||||
| chr6:89080570-89080784 | Common:1; Rare:91 | ||||
| chr6:89117962-89118085 | Common:1; Rare:52 | ||||
| chr6:89638723-89638839 | Common:3; Rare:38 | ||||
| chr6:89819758-89819871 | Rare:38 | ||||
| chr6:89829592-89829942 | Rare:89 | ||||
| chr6:93419546-93419777 | Common:1; Rare:64 |