chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34802652348026524AG9GENIChomozygous71875144
34802763748027638AG18GENIChomozygous71875146
34802907648029077CG13GENIChomozygous71875148
34802942348029424TA19GENIChomozygous71875150
34803007248030073TC31GENIChomozygous71875152
34803060748030608TG20GENIChomozygous71875154
34803087048030871CT16GENICpossibly homozygous71875156
34803253748032538AG12GENIChomozygous71875158
34803279248032793GT22GENIChomozygous71875160
34803342948033430GA12GENIChomozygous71875162
34803358948033590AG25GENIChomozygous71875164
34803412848034129GC22GENIChomozygous71875166
34803512548035126GC20GENIChomozygous71875168
34803631548036316CT36GENIChomozygous71875170
34803705348037054AC24GENIChomozygous71875172
34803815148038152CT13GENIChomozygous71875174
34804089048040891AT8GENIChomozygous71875180
34804298248042983TC35GENIChomozygous71875182
34804356548043566GA16GENIChomozygous71875184
34804441848044419GA27GENICpossibly homozygous71875186
34804460548044606CT18GENIChomozygous71875188
34804472448044725AG29GENIChomozygous71875190
34804488148044882AG48GENIChomozygous71875192
34804573348045734TC12GENIChomozygous71875194
34804601148046012CT20GENIChomozygous71875196
34804601248046013AG19GENIChomozygous71875198
34804626548046266GA18GENIChomozygous71875200
34804637948046380GA21GENIChomozygous71875202
34804712848047129AT13GENIChomozygous71875204
34804821648048217GA22GENIChomozygous71875206