chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5171388798171388799CA34GENIChomozygous114091781
5171389481171389482TC18GENIChomozygous114091783
5171394293171394294AC24GENIChomozygous114091787
5171394400171394401GA18GENIChomozygous114163256
5171394401171394402AG17GENIChomozygous118848020
5171394426171394427CT11GENIChomozygous118848022
5171394427171394428TG10GENIChomozygous118848024
5171394723171394724GA17GENIChomozygous114091791
5171396150171396151TC23GENIChomozygous118848028
5171396152171396153AT22GENIChomozygous114456383
5171396154171396155TC23GENIChomozygous114456384
5171396236171396237AC36GENICpossibly homozygous114091799
5171403150171403151TC27GENIChomozygous114091801
5171403151171403152TA26GENIChomozygous114091803
5171403152171403153TC26GENIChomozygous114091805
5171403154171403155TC27GENIChomozygous114091807
5171405403171405404GT23GENIChomozygous118938063
5171405404171405405TG23GENIChomozygous118938065