chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107034987270349873GA51GENIChomozygous116627614
107034993570349936GA55GENIChomozygous116627616
107035020670350207TC49GENIChomozygous116627618
107035178770351788GA31GENIChomozygous116627620
107035227470352275AG41GENIChomozygous116627622
107035315670353157GA26GENIChomozygous116627624
107035371470353715AG19GENIChomozygous116627626
107035706370357064CT34GENIChomozygous116627628
107035777570357776GA40GENIChomozygous116627630
107035792470357925GA51GENIChomozygous116627632
107035814370358144CT56GENIChomozygous116627634
107035815170358152GA53GENIChomozygous116627636
107035815570358156AG50GENIChomozygous116627638
107035819070358191CG55GENIChomozygous116627640
107035851170358512GT52GENIChomozygous116627642
107035915670359157AG27GENIChomozygous116627644
107035939170359392CT37GENIChomozygous116627646
107035945170359452TA40GENIChomozygous116627648
107035946370359464AG44GENIChomozygous116627650
107035966770359668AG34GENIChomozygous116627652
107035966870359669AG34GENIChomozygous116627654
107035969770359698GA26GENIChomozygous116627656
107035971270359713TC25GENIChomozygous116627658
107035971370359714GC25GENIChomozygous116627660
107036620570366206CA23GENIChomozygous116627662
107036646170366462TC30GENIChomozygous116627664
107036665470366655CG35GENIChomozygous116627666
107036666070366661GC37GENIChomozygous116627668
107036669770366698GA34GENIChomozygous116627670
107036671170366712CT33GENIChomozygous116627672