chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51316424313164244AG16GENIChomozygous114173716
51316456713164568AT38GENIChomozygous114173717
51316525313165254CT20GENIChomozygous114173718
51316537713165378AG19GENIChomozygous114173719
51316587013165871CT35GENIChomozygous114173720
51316610413166105AC18GENIChomozygous114173721
51316658813166589AG28GENIChomozygous114173722
51316664913166650CT24GENIChomozygous114173723
51316734313167344AG13GENIChomozygous113658119
51316743513167436AG17GENICpossibly homozygous114173724
51316764413167645CG14GENIChomozygous113658121
51316769513167696AG12GENICpossibly homozygous114173725
51316775413167755CA11GENIChomozygous114173726