chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1230114712230114713AT11GENICpossibly homozygous109451261
1230114898230114899GC16GENICpossibly homozygous109451262
1230115697230115698AG13GENIChomozygous109003790
1230115907230115908CA13GENIChomozygous109451263
1230116664230116665TG9GENIChomozygous109451264
1230116710230116711CT11GENIChomozygous109451265
1230117331230117332CT26GENIChomozygous109451266