chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10104147362104147375GGGGCTGGCGATT13GENICheterozygous129970945
10104148450104148451A43GENIChomozygous128855698
10104148456104148457G43GENIChomozygous128855699
10104148471104148472G45GENIChomozygous128855700
10104148484104148486AA47GENIChomozygous128855701
10104148493104148493CTAACTGC48GENIChomozygous128855702
10104148500104148501G49GENIChomozygous128855703
10104149517104149517C65GENIChomozygous128855704
10104155544104155545G77GENICpossibly homozygous128855705
10104149429104149430TC54GENIChomozygous116713724
10104149431104149432TC54GENIChomozygous116713726