chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64568655645686557GA30GENIChomozygous114784781
64568880945688810TA23GENIChomozygous114784783
64568975445689755AC18GENIChomozygous114784797
64568999945690000GA20GENIChomozygous114784801
64569007845690079AG23GENIChomozygous114784803
64569012845690129CT35GENIChomozygous114784805
64569035545690356GA38GENIChomozygous114784807
64569068945690690GA35GENIChomozygous114784809
64569077245690773TA29GENIChomozygous114784811
64569083045690831GA40GENIChomozygous114784813
64569113545691136CT24GENIChomozygous114784815
64569117445691175TC24GENIChomozygous114784817
64569117845691179TC23GENIChomozygous114784819
64569147245691473CT34GENIChomozygous114784821
64569155145691552AC36GENIChomozygous114784823
64569185745691858TC37GENIChomozygous114784825
64569197045691971GA44GENIChomozygous114784827
64569210645692107TC50GENIChomozygous114784829
64569217345692174AG44GENIChomozygous114784831
64569248645692487CG29GENIChomozygous114784833
64569280745692808CT29GENIChomozygous114784835
64569292045692921TG26GENIChomozygous114784837
64569330445693305GC19GENIChomozygous114784839
64569332445693325AG23GENIChomozygous114784841
64569337645693377AC37GENIChomozygous114784843
64569354245693543TC36GENIChomozygous114784845
64569354745693548CT34GENIChomozygous114784847
64569358145693582GA35GENIChomozygous114784849
64569367145693672TG36GENIChomozygous114784851
64569391045693911TC28GENIChomozygous114784853
64569412645694127AT20GENIChomozygous114784855
64569429445694295TC28GENIChomozygous114784857
64569430245694303TC29GENIChomozygous114784859
64569432645694327TC34GENIChomozygous114784861