chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
36763612967636130GA10GENIChomozygous111598141
36763724467637245GA22GENIChomozygous111598142
36763728367637284AC30GENIChomozygous111598143
36763750167637502GC20GENIChomozygous111598144
36763752867637529GA20GENIChomozygous111598145
36763859967638600TA20GENIChomozygous111598146
36763860367638604TA20GENIChomozygous111598147
36763929967639300TC23GENIChomozygous111598148
36763984567639846GA23GENICheterozygous111598149
36764017667640177CT26GENIChomozygous111598150
36764076767640768AC21GENIChomozygous111598151
36764124767641248TG19GENIChomozygous111598152
36764192667641927GC25GENIChomozygous111598153
36764199367641994CT24GENIChomozygous111598154
36764353867643539AG13GENIChomozygous111598155
36764401967644020AG22GENIChomozygous111598156
36764475667644757AG22GENIChomozygous111598157
36764496067644961AG18GENIChomozygous111598158
36764588767645888AT22GENIChomozygous111598159
36764625967646260TC26GENIChomozygous111598160
36764755567647556TC33GENIChomozygous111598161
36764787267647873GA23GENIChomozygous111598162
36764869967648700GA22GENIChomozygous111598163
36764878967648790GA28GENIChomozygous111915581
36764895167648952GC14GENIChomozygous111598164
36764895767648958CG13GENICpossibly homozygous111598165
36764896367648964CG19GENICheterozygous112232574
36764950967649510AG21GENIChomozygous111598166
36765047767650478GA19GENIChomozygous111598168
36765049967650500GA24GENIChomozygous111598169
36765063467650635GA26GENIChomozygous111598170
36765095067650951AG26GENIChomozygous111598171
36765226567652266GA32GENIChomozygous111598172
36765232667652327GA40GENIChomozygous111598173
36765244667652447GA20GENIChomozygous111598174
36765354567653546AG33GENIChomozygous111598175
36765361667653617AG28GENICpossibly homozygous111598176
36765374767653748GT21GENIChomozygous111598177
36765435867654359GA38GENIChomozygous111598178
36765449567654496CT10GENIChomozygous111598179
36765602367656024TC24GENIChomozygous111598180
36765698267656983AG33GENIChomozygous111598181
36765722367657224AG20GENIChomozygous111598182
36765727467657275AG21GENIChomozygous111598183
36765829467658295CT19GENIChomozygous111598184
36766047467660475CT11GENIChomozygous111598185
36766092767660928AG28GENIChomozygous111598186
36766096167660962CT24GENIChomozygous111598187
36766097567660976GA22GENIChomozygous111598188
36766107167661072CT29GENIChomozygous111598189
36766142567661426CT29GENIChomozygous111598190
36766159567661596GA16GENIChomozygous111598191
36766250367662504AG31GENIChomozygous111598192
36766301567663016AC18GENIChomozygous111598193
36766392867663929TC25GENICpossibly homozygous111598194
36766393167663932CT24GENICpossibly homozygous111598195
36766399867663999GA21GENIChomozygous111598196
36766406567664066AT13GENIChomozygous111598197
36766407567664076AT16GENIChomozygous111598198
36766470067664701TC19GENIChomozygous111598201
36766632967666330AG29GENIChomozygous111598202
36766714967667150GC32GENIChomozygous111598203
36766777467667775CT38GENIChomozygous111598204
36766851867668519GA34GENIChomozygous111598206
36766811667668117CT26GENIChomozygous111598205