chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5107836023107836024TC29GENIChomozygous114515448
5107840931107840932CT32GENIChomozygous114515450
5107842620107842621CT35GENIChomozygous113956446
5107843906107843907CT21GENICpossibly homozygous114515452
5107844127107844128AC37GENIChomozygous114515454
5107844357107844358AT36GENIChomozygous114236327
5107844789107844790CT19GENIChomozygous114236328
5107845111107845112CG10GENIChomozygous114515456
5107845265107845266CG16GENIChomozygous114236330
5107845283107845284GA21GENIChomozygous113956448
5107846524107846525TG23GENIChomozygous114515458
5107847344107847345CT10GENIChomozygous114515460
5107848543107848544TC28GENIChomozygous113956449
5107849329107849330AG24GENIChomozygous113956450
5107850077107850078GA33GENIChomozygous114515462
5107852132107852133AG27GENIChomozygous113956452
5107855256107855257AG27GENIChomozygous114236341
5107857364107857365TC35GENIChomozygous113956458