chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96754650467546505CT21GENIChomozygous117711622
96754790367547904CA24GENIChomozygous117711624
96754966567549666AG14GENIChomozygous117711626
96755100167551002AG14GENIChomozygous117551913
96755194167551942TG12GENIChomozygous117711630
96755227367552274TC10GENIChomozygous117551919
96755493967554940AG20GENIChomozygous117551931
96755620967556210TG16GENIChomozygous117551939
96755663767556638AG28GENIChomozygous117711632
96755733067557331GA23GENIChomozygous117711634
96755950767559508GC23GENIChomozygous117551949
96756157067561571TC16GENIChomozygous117711636
96756206167562062CT12GENIChomozygous117711638
96756408067564081GC14GENIChomozygous117711640
96756518967565190CT22GENICheterozygous117824482
96756801567568016AG10GENIChomozygous117711644
96756875867568759GA16GENIChomozygous117711646
96757031567570316CG23GENICpossibly homozygous117711648
96757075667570757TA15GENIChomozygous117711650
96757093867570939AG13GENIChomozygous117711652
96757336167573362TA8GENIChomozygous117711654