chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134803210948032110AC11GENIChomozygous114548661
134803300848033009CG11GENIChomozygous114615401
134803410748034108GA14GENIChomozygous114615402
134803668748036688TC18GENIChomozygous114548665
134803676248036763GA14GENIChomozygous114615403
134803714548037146GC16GENIChomozygous114615404
134803745348037454CT14GENIChomozygous114615405
134803763148037632GT16GENIChomozygous114615406
134803781448037815TG17GENIChomozygous114548668
134803793848037939AG15GENIChomozygous114548670
134803827848038279AG19GENIChomozygous114548671
134803885248038853CT21GENIChomozygous114548672
134803895948038960GA14GENIChomozygous114615407
134803916748039168GC10GENIChomozygous114548673
134803942748039428CT26GENIChomozygous114615408
134803968848039689AG24GENIChomozygous114548674
134803971548039716TC23GENIChomozygous114548675
134804220648042207TC21GENIChomozygous114548676
134804222948042230GA24GENIChomozygous114615409
134804319348043194AG22GENIChomozygous114615410
134804341048043411GA26GENIChomozygous114615411
134804357448043575GT19GENIChomozygous114548678
134804410148044102TC15GENIChomozygous114615412
134804436848044369TC13GENIChomozygous114615413
134804473648044737AG18GENIChomozygous114548681
134804553448045535CT19GENIChomozygous114548682
134804617448046175AC13GENIChomozygous114548683
134804640948046410AT10GENIChomozygous114548684
134804730648047307AG16GENIChomozygous114548685
134804855548048556AG16GENIChomozygous114548686
134805192448051925GT14GENIChomozygous114615414
134805332948053330TC17GENIChomozygous114548690
134805543348055434AG11GENIChomozygous114548695