chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761598617615987TC22GENIChomozygous777096575
141761702817617029CA20GENIChomozygous777096576
141762106317621064TC33GENIChomozygous777096577
141762138217621383TC44GENIChomozygous777096578
141762256517622566TA26GENIChomozygous777096579
141762303117623032CT34GENICpossibly homozygous777096580
141762436417624365CT52GENIChomozygous777096581
141762439017624391TC58GENIChomozygous777096582
141762442617624427CG60GENIChomozygous777096583
141762588517625886AG26GENIChomozygous777096584
141762981017629811AG21GENIChomozygous777096585
141762983717629838TC23GENIChomozygous777096586
141762984117629842TC22GENIChomozygous777096587
141762992517629926AG37GENIChomozygous777096588
141763052217630523TA24GENIChomozygous777096589
141763065017630651TG16GENIChomozygous777096590