| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:85643296-85643495 | Rare:75 | ||||
| chr6:87155248-87155604 | Rare:92 | ||||
| chr6:87472832-87473004 | Common:1; Rare:59; Clinvar (benign):4 | ||||
| chr6:87589924-87590160 | Common:2; Rare:116; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:87702215-87702385 | Rare:64 | ||||
| chr6:88047674-88047868 | Common:2; Rare:56 | ||||
| chr6:88963585-88963830 | Common:2; Rare:83 | ||||
| chr6:89081029-89081098 | Rare:33 | ||||
| chr6:89117943-89118087 | Common:1; Rare:57 | ||||
| chr6:89145983-89146090 | Rare:32 | ||||
| chr6:89638434-89638532 | Common:1; Rare:18 | ||||
| chr6:89638712-89638845 | Common:3; Rare:48 | ||||
| chr6:89819688-89819877 | Rare:62 | ||||
| chr6:89829595-89829924 | Rare:81 | ||||
| chr6:90586927-90587091 | Common:1; Rare:52 |