chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221673820221673821GA26GENIChomozygous109056672
1221673875221673876TC27GENIChomozygous108545019
1221674126221674127GC24GENIChomozygous108545021
1221674408221674409GA31GENIChomozygous108545023
1221677431221677432TC15GENIChomozygous108545029
1221678311221678312GA28GENIChomozygous108995099
1221678794221678795CT27GENIChomozygous108995100
1221678955221678956GT30GENIChomozygous108995101
1221679320221679321CA21GENIChomozygous108995102
1221679731221679732CT35GENIChomozygous108995103
1221681844221681845GA23GENIChomozygous108545033
1221681869221681870TC26GENIChomozygous108545035
1221682384221682385AG29GENIChomozygous108545037
1221683624221683625GA30GENIChomozygous108545039
1221684609221684610CA23GENICpossibly homozygous108995104
1221685443221685444A21GENIChomozygous131782612
1221685854221685855CT29GENIChomozygous108545041
1221687439221687440TC34GENIChomozygous108545043
1221687550221687551CT24GENIChomozygous108545045
1221688772221688773GT20GENIChomozygous108545047
1221688847221688848GA16GENIChomozygous108995105
1221690342221690343AG33GENIChomozygous108545051
1221691169221691170AG20GENIChomozygous108545055
1221691510221691511TG30GENIChomozygous108995106