| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:89638712-89638831 | Common:3; Rare:44 | ||||
| chr6:89819699-89819863 | Rare:57 | ||||
| chr6:89829614-89829914 | Rare:70 | ||||
| chr6:93419538-93419744 | Common:1; Rare:62 | ||||
| chr6:95577398-95577543 | Common:3; Rare:38 | ||||
| chr6:96521723-96521871 | Common:3; Rare:69 | ||||
| chr6:96897821-96898012 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:99425214-99425494 | Common:2; Rare:83 | ||||
| chr6:100881265-100881482 | Common:5; Rare:89 | ||||
| chr6:104859899-104859983 | Rare:21 | ||||
| chr6:106086192-106086386 | Rare:52 | ||||
| chr6:106325531-106325892 | Common:1; Rare:117 | ||||
| chr6:106629462-106629588 | Common:1; Rare:25 | ||||
| chr6:107958121-107958399 | Common:1; Rare:83; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:108260765-108260815 | Rare:14 |