chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85803176858031769G24GENIChomozygous141015290
85803177058031771CA23GENIChomozygous141025360
85803201758032018CT12GENIChomozygous141025361
85803241058032411GA19GENIChomozygous141025362
85803477358034774CG32GENIChomozygous141025363
85803504258035043AG19GENIChomozygous141025364
85803544158035445AATG4GENIChomozygous141015291
85803638258036383TA29GENIChomozygous141025365
85803663858036639CT21GENIChomozygous141025366
85803668158036682GC17GENIChomozygous141025367
85803700558037006TA14GENIChomozygous141025368
85803700658037007GA13GENIChomozygous141025369
85803790058037900ACAG7GENIChomozygous141015292
85803812858038129A26GENIChomozygous141015293
85803902158039022GA23GENIChomozygous141025370
85804007058040071TC16GENIChomozygous141025371
85804056958040569AAT27GENIChomozygous141015294
85804101758041018CA18GENIChomozygous141025372
85804123058041233CAC4GENIChomozygous141015295
85804123558041237AG4GENIChomozygous141015296
85804154358041544AG14GENIChomozygous141025373
85804185758041858TG23GENIChomozygous141025374
85804217258042173CT19GENIChomozygous141025375
85804282758042828AG29GENIChomozygous141025376
85804372358043724GA27GENIChomozygous141025377
85804374058043741TC24GENIChomozygous141025378
85804446258044462AG14GENIChomozygous141015297
85804446658044466AGAGACAG15GENIChomozygous141015298
85804514458045145AT20GENIChomozygous141025379
85804559558045595AGC19GENIChomozygous141015299
85804585758045858AG20GENIChomozygous141025380
85804607758046077G24GENIChomozygous141015300
85804663158046641GGCATGAGGC26GENIChomozygous141015301
85804669258046693GC26GENIChomozygous141025381
85804789358047894TC8GENIChomozygous141025382
85804864858048649CT25GENIChomozygous141025383