Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:78122-78287 | Common:3; Rare:60 | ||||
chr16:234743-234842 | Rare:43 | ||||
chr16:397109-397312 | Common:4; Rare:55 | ||||
chr16:684326-684464 | Common:2; Rare:72 | ||||
chr16:726900-727130 | Common:4; Rare:59 | ||||
chr16:1771499-1771860 | Common:3; Rare:142 | ||||
chr16:1782510-1782850 | Common:4; Rare:114 | ||||
chr16:1943155-1943499 | Common:1; Rare:107 | ||||
chr16:1964817-1965061 | Common:6; Rare:108 | ||||
chr16:1971915-1972106 | Common:1; Rare:55 | ||||
chr16:2047795-2048043 | Rare:114; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2268071-2268193 | Common:1; Rare:54 | ||||
chr16:2474987-2475136 | Rare:49 | ||||
chr16:2682367-2682609 | Rare:107 | ||||
chr16:2777001-2777377 | Common:2; Rare:136 |