chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221673875221673876TC12GENIChomozygous108545019
1221674126221674127GC26GENIChomozygous108545021
1221674408221674409GA36GENIChomozygous108545023
1221677324221677325AG21GENIChomozygous120595016
1221677431221677432TC30GENIChomozygous108545029
1221679320221679321CA29GENIChomozygous108995102
1221679731221679732CT32GENIChomozygous108995103
1221681844221681845GA20GENIChomozygous108545033
1221681869221681870TC20GENIChomozygous108545035
1221682281221682282CT17GENIChomozygous120595018
1221682384221682385AG22GENIChomozygous108545037
1221683143221683144GA32GENIChomozygous120595020
1221684960221684961CT36GENIChomozygous120595022
1221685854221685855CT26GENIChomozygous108545041
1221686903221686904AG27GENIChomozygous120595024
1221687286221687287CT31GENIChomozygous120595026
1221687439221687440TC41GENIChomozygous108545043
1221687550221687551CT30GENIChomozygous108545045
1221688144221688145CT27GENIChomozygous120595028
1221688772221688773GT25GENIChomozygous108545047
1221690342221690343AG22GENIChomozygous108545051
1221691169221691170AG31GENIChomozygous108545055
1221692307221692308TC27GENIChomozygous120595030