chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116066814660668147TC25GENIChomozygous50797058
116066829460668295C-16GENIChomozygous50797060
116067127660671277CT23GENIChomozygous50797062
116067148060671481GA16GENIChomozygous50797064
116067156960671570GA20GENIChomozygous50797066
116067163960671640TC24GENIChomozygous50797068
116067168260671683TC24GENIChomozygous50797070
116067171160671712TA24GENIChomozygous50797071
116067172160671722CT24GENIChomozygous50797073
116067217260672173GA28GENIChomozygous50797075
116067223560672236AG23GENIChomozygous50797077
116067244160672442TC21GENIChomozygous50797079
116067286460672865TC29GENIChomozygous50797081
116067291760672918TA26GENIChomozygous50797083
116067293760672938GA24GENIChomozygous50797085
116067304060673041CT16GENIChomozygous50797087
116067306260673063TC13GENIChomozygous50797089
116067370760673708AG30GENIChomozygous50797091
116067385860673859CG32GENIChomozygous50797093
116067402560674026GA22GENIChomozygous50797095
116067403060674031CA23GENIChomozygous50797097
116067436960674370AG18GENIChomozygous50797099
116067484160674842GA21GENIChomozygous50797100
116067529160675292GT33GENIChomozygous50797102
116067532060675321CT38GENIChomozygous50797104
116067657160676572TC41GENIChomozygous50797106
116067664160676642CT35GENIChomozygous50797108
116067703160677032TC28GENIChomozygous50797110
116067714460677145AG25GENIChomozygous50797112
116067728660677287AG26GENIChomozygous50797114
116067744860677449AG31GENIChomozygous50797116
116067757960677580CT19GENIChomozygous50797118
116067775760677758GA18GENIChomozygous50797120
116067783260677833GA16GENIChomozygous50797121
116067823760678239AA--1GENIChomozygous50882092
116067864960678650CT27GENIChomozygous50797123
116067884060678842TC--17GENIChomozygous50797125
116067948160679482GA20GENIChomozygous50797127
116067962760679628AG24GENIChomozygous50797129
116067988760679888CT22GENIChomozygous50797131
116068067160680672TC25GENIChomozygous50797133