chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171707957171707958CA39GENICpossibly homozygous60943319
1171707963171707964GC39GENIChomozygous60943320
1171708171171708172GA63GENIChomozygous60943321
1171709090171709092GG--20GENIChomozygous60943322
1171709381171709382GA66GENIChomozygous60943323
1171710179171710180GA46GENIChomozygous60943324
1171711756171711757CT50GENIChomozygous60943325
1171713005171713006GA66GENIChomozygous60943326
1171713098171713099GA64GENIChomozygous60943327