chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
389835598983560CT37GENIChomozygous811364153
389838728983873TA15GENIChomozygous811364154
389840348984035CT27GENIChomozygous811364155
389843058984306TA31GENIChomozygous811364156
389846318984632CT32GENIChomozygous811364157
389847268984727TC24GENIChomozygous811364158
389847288984729GA24GENIChomozygous811364159
389849628984963GA24GENIChomozygous811364160
389850108985011CT31GENIChomozygous811364161
389850278985028AG28GENIChomozygous811364162
389850748985075GA20GENIChomozygous811364163
389854338985434CT19GENICheterozygous811364164
389863498986350CA21GENIChomozygous811364165
389873688987369AC11GENICheterozygous811364166
389875288987529GC9GENIChomozygous811364167
389877778987778CT12GENIChomozygous811364168
389878298987830TC12GENIChomozygous811364169
389880188988019AC6GENICheterozygous811364170
389882008988201GC3GENIChomozygous811364171
389887368988737GA26GENIChomozygous811364172
389893458989346TC15GENIChomozygous811364173
389897048989705GA16GENIChomozygous811364174
389903258990326TC41GENIChomozygous811364175
389914098991410TC32GENIChomozygous811364176
389921188992119TC33GENIChomozygous811364177
389923788992379AG28GENIChomozygous811364178
389926378992638AG31GENIChomozygous811364179
389930228993023CT33GENIChomozygous811364180
389953198995320CT21GENICheterozygous811364181
389958388995839GA22GENIChomozygous811364182
389973408997341AG36GENIChomozygous811364183
389982388998239CT41GENIChomozygous811364184
389984358998436TC47GENIChomozygous811364185
389993248999325GA34GENIChomozygous811364186
389993448999345AG37GENICpossibly homozygous811364187
390007959000796GA175GENICheterozygous811364188
390029759002976CT38GENIChomozygous811364189
390034199003420GA41GENIChomozygous811364190
390065329006533TC26GENIChomozygous811364191
390067139006714CT31GENIChomozygous811364192
390080249008025CT33GENIChomozygous811364193
390094699009470AG25GENICpossibly homozygous811364194
390123439012344CT36GENIChomozygous811364195