chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
43238812432388125GA38GENIChomozygous112570560
43238822932388230TG36GENIChomozygous112570562
43238870032388701TC31GENIChomozygous112570564
43238945332389454GC16GENIChomozygous112570566
43239102032391021GT36GENIChomozygous112570568
43239104732391048AT33GENIChomozygous112570570
43239107732391078TC27GENIChomozygous112570572
43239111532391116AG30GENIChomozygous112570574
43239130032391301TC8GENIChomozygous113092720
43239133132391332TC17GENIChomozygous112570578
43239140832391409TC25GENIChomozygous112570582
43239146032391461CA19GENICpossibly homozygous113092722
43239163132391632GC26GENICpossibly homozygous112570584