chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2316800223168003GA10GENIChomozygous108239705
X2316880423168805TC14GENIChomozygous108239707
X2316938423169385TG7GENIChomozygous108239709
X2317085623170857TC8GENIChomozygous108239715
X2317178723171788CT11GENIChomozygous108239717
X2317313023173131CG4GENIChomozygous108524001
X2317328023173281CA7GENIChomozygous119910358
X2317328123173282TA7GENICpossibly homozygous119990129
X2317328723173288CA8GENIChomozygous108524011
X2317330623173307AG10GENIChomozygous108239719
X2317331323173314CT10GENIChomozygous108239721
X2317332323173324AC10GENIChomozygous108239723
X2317332723173328GC12GENIChomozygous108239725
X2317333423173335AC13GENIChomozygous108239727
X2317401323174014CT11GENIChomozygous108239729
X2317432323174324GA16GENIChomozygous108239731
X2317554323175544AG13GENIChomozygous119910359
X2317567523175676AT10GENIChomozygous108544976
X2317607923176080CA6GENIChomozygous108730950
X2317610123176102AC7GENIChomozygous119910360
X2317841823178419AG16GENIChomozygous108239737
X2317614623176147AG10GENIChomozygous119910361
X2317732623177327AG19GENIChomozygous108239733
X2317797623177977CG6GENIChomozygous108239735
X2318018523180186GA4GENIChomozygous108439834
X2318020823180209AG6GENIChomozygous108439837
X2318063223180633TC12GENIChomozygous108239739
X2318087523180876GT16GENIChomozygous108239741
X2318101923181020GA10GENIChomozygous108239747
X2318142823181429TC10GENIChomozygous108239753
X2318149923181500CT13GENIChomozygous108239755
X2318547023185471AG11GENIChomozygous108239761