chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8128779808128779809GA54GENIChomozygous116722030
8128780153128780154AC62GENIChomozygous116722031
8128780206128780207TC63GENIChomozygous116722032
8128780251128780252AG67GENIChomozygous116722033
8128780392128780404GAATGAATGAAT49GENIChomozygous128647241
8128780777128780778CG54GENIChomozygous116722034
8128781026128781026AC61GENIChomozygous128647242
8128781038128781038AGAA62GENIChomozygous128647243
8128781044128781044AG61GENIChomozygous128647244
8128781073128781074CG58GENIChomozygous116901725
8128781075128781076GC59GENIChomozygous123065960
8128781389128781390GA66GENIChomozygous116722035
8128781430128781431TC64GENIChomozygous116722036
8128781487128781488TC63GENIChomozygous116722037
8128781643128781644CT63GENIChomozygous116722038
8128782171128782172GA62GENIChomozygous116722039
8128780943128780944CT50GENICpossibly homozygous118151585
8128782321128782322CT51GENIChomozygous116722040
8128782503128782504CT32GENIChomozygous118151587