chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85336602653366027CA10GENIChomozygous785913557
85336702053367021GA24GENIChomozygous785913558
85336731453367315TC33GENIChomozygous785913559
85336788453367885AG23GENIChomozygous785913560
85336797553367976AG18GENIChomozygous785913561
85336804753368048AT20GENIChomozygous785913562
85336809253368093CT27GENIChomozygous785913563
85336815753368158GA27GENIChomozygous785913564
85336816753368168TC27GENIChomozygous785913565
85336840253368403GA19GENIChomozygous785913566
85336884253368843AG13GENIChomozygous785913567
85336907653369077GA19GENIChomozygous785913568
85336983853369839TC29GENIChomozygous785913569
85336993353369934GA27GENIChomozygous785913570
85337013753370138AG19GENIChomozygous785913571
85337043353370434GA23GENIChomozygous785913572
85337337753373378TC23GENIChomozygous785913573
85337390953373910CG23GENIChomozygous785913574
85337583253375833TC14GENIChomozygous785913575
85337653253376533CT17GENIChomozygous785913576
85337653353376534AG18GENIChomozygous785913577
85337677153376772CA21GENIChomozygous785913578
85337776553377766GT15GENIChomozygous785913579
85338242553382426GA24GENIChomozygous785913580
85338252053382521AG26GENIChomozygous785913581
85338342253383423GA12GENIChomozygous785913582
85338359753383598AC10GENIChomozygous785913583
85338484553384846CT23GENIChomozygous785913584
85338492753384928CT27GENIChomozygous785913585
85338653553386536TG38GENIChomozygous785913586
85338719553387196TA27GENIChomozygous785913587
85338760653387607TG32GENIChomozygous785913588
85338770953387710CT27GENICpossibly homozygous785913589
85338784853387849GA17GENIChomozygous785913590
85338878353388784AT22GENIChomozygous785913591
85338929253389293TA24GENIChomozygous785913592
85339007453390075TC23GENIChomozygous785913593
85339008253390083CT23GENIChomozygous785913594