chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116066814660668147TC14GENIChomozygous50797058
116066829460668295C-5GENIChomozygous50797060
116067127660671277CT29GENIChomozygous50797062
116067148060671481GA26GENIChomozygous50797064
116067156960671570GA25GENIChomozygous50797066
116067163960671640TC30GENIChomozygous50797068
116067168260671683TC27GENIChomozygous50797070
116067171160671712TA25GENIChomozygous50797071
116067172160671722CT25GENIChomozygous50797073
116067217260672173GA28GENIChomozygous50797075
116067223560672236AG18GENIChomozygous50797077
116067244160672442TC22GENIChomozygous50797079
116067286460672865TC12GENIChomozygous50797081
116067291760672918TA19GENIChomozygous50797083
116067293760672938GA18GENIChomozygous50797085
116067304060673041CT20GENIChomozygous50797087
116067306260673063TC22GENIChomozygous50797089
116067370760673708AG19GENIChomozygous50797091
116067436960674370AG26GENIChomozygous50797099
116067385860673859CG28GENIChomozygous50797093
116067402560674026GA21GENIChomozygous50797095
116067403060674031CA20GENIChomozygous50797097
116067484160674842GA15GENIChomozygous50797100
116067529160675292GT30GENIChomozygous50797102
116067532060675321CT31GENIChomozygous50797104
116067657160676572TC15GENIChomozygous50797106
116067664160676642CT20GENIChomozygous50797108
116067703160677032TC17GENIChomozygous50797110
116067714460677145AG25GENIChomozygous50797112
116067728660677287AG23GENIChomozygous50797114
116067744860677449AG22GENIChomozygous50797116
116067757960677580CT15GENIChomozygous50797118
116067775760677758GA26GENIChomozygous50797120
116067783260677833GA14GENIChomozygous50797121
116067823760678239AA--20GENIChomozygous50882092
116067864960678650CT29GENIChomozygous50797123
116067884060678842TC--21GENIChomozygous50797125
116067948160679482GA21GENIChomozygous50797127
116067962760679628AG20GENIChomozygous50797129
116067988760679888CT15GENIChomozygous50797131
116068067160680672TC22GENIChomozygous50797133