chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142293282322932824GA18GENIChomozygous976966544
142293304222933043CT19GENIChomozygous976966545
142293466522934666AG25GENIChomozygous976966546
142293586922935870GA20GENICheterozygous976966547
142293587122935872TA15GENICheterozygous976966548
142293636622936367GA12GENIChomozygous976966549
142293713922937140AG7GENICpossibly homozygous976966550
142293739722937398GA21GENIChomozygous976966551
142293764622937647TA33GENIChomozygous976966552
142293768322937684TC31GENIChomozygous976966553
142294094922940950AG24GENIChomozygous976966554
142294134322941344CA27GENIChomozygous976966555
142294277722942778CA13GENIChomozygous976966556
142294389522943896AG30GENIChomozygous976966557
142294402922944030TA31GENIChomozygous976966558
142294751922947520CA16GENIChomozygous976966559
142294752122947522AC15GENIChomozygous976966560
142295235922952360CG31GENIChomozygous976966561
142295552222955523CT43GENIChomozygous976966562
142295557922955580GT47GENIChomozygous976966563