| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:106325616-106325976 | Common:1; Rare:132 | ||||
| chr6:106629400-106629701 | Common:5; Rare:83 | ||||
| chr6:106975170-106975421 | Common:1; Rare:70 | ||||
| chr6:107459522-107459742 | Common:2; Rare:52 | ||||
| chr6:108074647-108074838 | Rare:65; Clinvar:1 | ||||
| chr6:108294788-108295071 | Common:1; Rare:75 | ||||
| chr6:109009451-109009677 | Common:2; Rare:73 | ||||
| chr6:109095418-109095561 | Rare:29 | ||||
| chr6:109382394-109382815 | Common:6; Rare:135; Clinvar (benign):1 | ||||
| chr6:109691158-109691361 | Common:3; Rare:45; Clinvar:5; Clinvar (benign):3 | ||||
| chr6:110179616-110179702 | Rare:34 | ||||
| chr6:110874616-110874816 | Common:4; Rare:65 | ||||
| chr6:110958616-110958788 | Common:4; Rare:66 | ||||
| chr6:110981910-110982100 | Common:3; Rare:89 | ||||
| chr6:111483748-111483769 | Rare:11 |