chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2257608042257608043CA6GENIChomozygous110864346
2257610565257610566CT18GENIChomozygous111196942
2257610881257610882GA10GENIChomozygous110412177
2257611490257611491AC24GENIChomozygous111196944
2257613876257613877GA20GENIChomozygous110412181
2257616438257616439AT14GENIChomozygous111043875
2257616880257616881TC23GENIChomozygous110412187
2257619052257619053CT22GENIChomozygous111196946
2257619792257619793AG22GENIChomozygous111043879
2257620338257620339AC15GENIChomozygous110412191
2257621763257621764AG19GENIChomozygous110412193
2257622429257622430TC6GENIChomozygous110412197
2257622569257622570TC16GENIChomozygous110412199
2257622657257622658TC11GENIChomozygous110412201
2257623130257623131AG18GENIChomozygous111043880
2257626425257626426AG13GENIChomozygous111043882
2257627641257627642CA26GENICpossibly homozygous111043884
2257628262257628263TC18GENIChomozygous110412205
2257629623257629624AG24GENIChomozygous110412209
2257630111257630112AG31GENIChomozygous110412211
2257631926257631927CT17GENICpossibly homozygous111196948
2257633127257633128TA10GENIChomozygous111043886
2257635344257635345CT20GENIChomozygous111196950
2257640652257640653TC24GENIChomozygous110412217
2257641126257641127AC9GENIChomozygous111043898
2257643206257643207CA25GENIChomozygous110412221
2257646730257646731AT9GENIChomozygous111196952
2257646903257646904CA19GENIChomozygous110412227
2257647014257647015AC15GENIChomozygous111196954
2257651086257651087TC22GENIChomozygous110412235
2257655630257655631AG27GENIChomozygous110412237
2257655660257655661CT27GENIChomozygous111196956
2257657150257657151TC18GENIChomozygous110412243
2257661195257661196AG21GENIChomozygous110412248
2257664804257664805TC32GENIChomozygous110412260
2257667974257667975TC18GENIChomozygous111196958
2257669891257669892TC27GENIChomozygous110412270