chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2317178723171788CT10GENIChomozygous108239717
X2317332723173328GC10GENIChomozygous108239725
X2317333423173335AC11GENIChomozygous108239727
X2317401323174014CT11GENICpossibly homozygous108239729
X2318087523180876GT6GENIChomozygous108239741
X2318091923180920AG7GENIChomozygous108239743
X2318092223180923GA7GENIChomozygous108239745
X2318101923181020GA11GENIChomozygous108239747
X2318102323181024CG11GENIChomozygous108544978
X2318109323181094CT13GENIChomozygous108239749
X2318109523181096TG14GENIChomozygous108239751
X2318142823181429TC16GENIChomozygous108239753
X2318164723181648AC16GENIChomozygous108544980
X2318167523181676CG16GENIChomozygous108239757
X2318167623181677GC16GENIChomozygous108239759
X2318430223184303AG14GENICpossibly homozygous108544982
X2318452023184521TC13GENICpossibly homozygous108544984
X2318529323185294TC15GENIChomozygous108544986
X2318547023185471AG10GENIChomozygous108239761
X2318590923185910AT11GENIChomozygous108544988
X2318700223187003TC19GENICpossibly homozygous108544990
X2317691123176912AT15GENIChomozygous108701208