chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
22327610523276106TG43GENIChomozygous109641247
22327705523277056CT32GENIChomozygous109641249
22327706223277063CT31GENIChomozygous110673317
22327755723277558GA35GENIChomozygous110673319
22327804623278047CG18GENIChomozygous110673321
22327849523278496TC54GENIChomozygous109641253
22327855323278554AG49GENIChomozygous109641257
22327924823279249TC29GENIChomozygous109641259
22327975023279751CT44GENICpossibly homozygous109641263
22327978023279781CT41GENIChomozygous109641265
22328136723281368CT29GENIChomozygous109641267
22328145423281455AC29GENICpossibly homozygous109641269
22328174623281747TC34GENICheterozygous110673324
22328183423281835CT44GENIChomozygous110673326
22328272423282725AG33GENIChomozygous109641277
22328336523283366GT44GENICpossibly homozygous110673328
22328430623284307TC36GENICpossibly homozygous109641279
22328437423284375GT35GENICpossibly homozygous109641281
22328441123284412AG33GENIChomozygous109641283
22328490823284909GC47GENIChomozygous110673330
22328527423285275GA32GENIChomozygous110673332
22328634123286342TC37GENIChomozygous109641291
22328663623286637AC54GENIChomozygous109641293
22328678423286785CT63GENICpossibly homozygous110673334
22328679323286794TC63GENICpossibly homozygous110673336
22328686723286868AG32GENIChomozygous109641295
22328714923287150AG34GENIChomozygous109641297
22328731923287320TC53GENIChomozygous109641299
22328774323287744AG34GENIChomozygous109641301
22328785523287856TC35GENICpossibly homozygous109641303
22328834623288347CT32GENIChomozygous110673338