chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1166111785166111786TC27GENIChomozygous108356098
1166112054166112055AC39GENIChomozygous109342271
1166112744166112745AG28GENIChomozygous108356099
1166112767166112768GA27GENIChomozygous108356100
1166112971166112972TC34GENIChomozygous108356101
1166113703166113704TC28GENIChomozygous108356102
1166114044166114045AT43GENIChomozygous108356103
1166115120166115121GT33GENIChomozygous108356104
1166115794166115795CT38GENIChomozygous108356105
1166117402166117403GC15GENIChomozygous108356106
1166117835166117836GA30GENICheterozygous109342273
1166118009166118010AC26GENIChomozygous108356107
1166118904166118905CT43GENIChomozygous108356108
1166120076166120077GA54GENIChomozygous108356109
1166120611166120612TC26GENIChomozygous108356110
1166123292166123293TC28GENIChomozygous108356111
1166124164166124165TC31GENIChomozygous108356112
1166124670166124671GA21GENIChomozygous108356113
1166126624166126625GC39GENIChomozygous108356115
1166129476166129477AG29GENIChomozygous108356117
1166130094166130095TC32GENIChomozygous108356119
1166130239166130240AG28GENIChomozygous108356120
1166130488166130489GA36GENIChomozygous108356121
1166130647166130648GA51GENIChomozygous108356122
1166130856166130857CA39GENIChomozygous108356123
1166131521166131522TC37GENIChomozygous108356124
1166135467166135468CT41GENIChomozygous108356126
1166136273166136274GA24GENIChomozygous108356127
1166138477166138478GA37GENIChomozygous108356128