chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34802652348026524AG13GENIChomozygous71875144
34802763748027638AG28GENICpossibly homozygous71875146
34802907648029077CG20GENIChomozygous71875148
34802942348029424TA14GENIChomozygous71875150
34802963548029635T24GENIChomozygous74010923
34803007248030073TC12GENIChomozygous71875152
34803060748030608TG15GENIChomozygous71875154
34803087048030871CT15GENIChomozygous71875156
34803114448031146AA23GENICheterozygous73365229
34803234448032345A24GENICheterozygous73365231
34803253748032538AG18GENIChomozygous71875158
34803342948033430GA17GENIChomozygous71875162
34803358948033590AG12GENIChomozygous71875164
34803412848034129GC26GENIChomozygous71875166
34803512548035126GC28GENIChomozygous71875168
34803559548035595GA18GENICheterozygous74010926
34803631548036316CT20GENIChomozygous71875170
34803705348037054AC19GENIChomozygous71875172
34803883848038839TG10GENIChomozygous71875176
34804089048040891AT13GENIChomozygous71875180
34804298248042983TC12GENIChomozygous71875182
34804356548043566GA23GENIChomozygous71875184
34804441848044419GA19GENIChomozygous71875186
34804460548044606CT23GENIChomozygous71875188
34804472448044725AG17GENIChomozygous71875190
34804488148044882AG15GENIChomozygous71875192
34804573348045734TC19GENIChomozygous71875194
34804601148046012CT19GENIChomozygous71875196
34804601248046013AG19GENIChomozygous71875198
34804626548046266GA15GENIChomozygous71875200
34804637948046380GA22GENIChomozygous71875202
34804712848047129AT23GENIChomozygous71875204
34804821648048217GA23GENIChomozygous71875206
34804885548048856GA8GENIChomozygous74010929