chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1175663674175663675CT19GENIChomozygous109352234
1175664052175664053TG4GENIChomozygous108757111
1175664061175664062GT3GENICheterozygous125406214
1175665115175665116AG24GENICpossibly homozygous108394702
1175665927175665928TC11GENIChomozygous108757113
1175666149175666150CT23GENIChomozygous108394704
1175666223175666224AG17GENIChomozygous108394706
1175667009175667010TC19GENIChomozygous108394707
1175668509175668510AG20GENIChomozygous108394711
1175669069175669070GA27GENIChomozygous109352238
1175669848175669849GA23GENIChomozygous108394713
1175673368175673369TC20GENIChomozygous108394719
1175673481175673482AG14GENIChomozygous108394721
1175673914175673915TA6GENIChomozygous120474792
1175674913175674914CT15GENIChomozygous108394725
1175675286175675287CT10GENIChomozygous108394727
1175675339175675340CT18GENIChomozygous108394729