Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:108260764-108261021 | Rare:113 | ||||
chr6:109009440-109009666 | Common:2; Rare:73 | ||||
chr6:109095402-109095557 | Rare:34 | ||||
chr6:109381686-109381756 | Common:1; Rare:19 | ||||
chr6:109382209-109382259 | Rare:22 | ||||
chr6:109382364-109382596 | Common:5; Rare:95; Clinvar (benign):1 | ||||
chr6:109455774-109456084 | Common:1; Rare:72 | ||||
chr6:109691161-109691352 | Common:3; Rare:43; Clinvar:4; Clinvar (benign):3 | ||||
chr6:110179962-110180184 | Common:2; Rare:64 | ||||
chr6:110958574-110958788 | Common:5; Rare:77 | ||||
chr6:110981959-110982113 | Common:2; Rare:78 | ||||
chr6:111259210-111259366 | Common:2; Rare:51 | ||||
chr6:112087418-112087667 | Rare:83 | ||||
chr6:116254044-116254242 | Common:5; Rare:55 | ||||
chr6:116279444-116279479 | Common:1; Rare:14 |