chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
43238812432388125GA17GENIChomozygous112570560
43238822932388230TG13GENIChomozygous112570562
43238870032388701TC16GENIChomozygous112570564
43238945332389454GC14GENICpossibly homozygous112570566
43239102032391021GT16GENIChomozygous112570568
43239104732391048AT10GENIChomozygous112570570
43239107732391078TC13GENIChomozygous112570572
43239111532391116AG13GENIChomozygous112570574
43239130032391301TC11GENIChomozygous113092720
43239133132391332TC9GENIChomozygous112570578
43239140832391409TC12GENIChomozygous112570582
43239146032391461CA11GENIChomozygous113092722
43239163132391632GC18GENIChomozygous112570584