chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1142087849142087850AG47GENIChomozygous109049763
1142088675142088676C41GENICpossibly homozygous130520089
1142091637142091638GA46GENIChomozygous108937351
1142092365142092366T37GENIChomozygous127439686
1142095281142095282AG51GENIChomozygous108262659
1142096564142096565GT51GENIChomozygous109049765
1142097858142097859GT11GENIChomozygous108262661
1142098430142098431TG8GENIChomozygous108743914
1142098434142098435TG8GENIChomozygous108743916
1142100410142100411TG47GENIChomozygous108262663
1142100485142100486TC50GENIChomozygous109327838
1142100490142100491AC49GENIChomozygous109049770
1142101397142101398GC59GENIChomozygous109049771
1142104770142104771TC54GENIChomozygous108262665
1142105585142105586GA57GENIChomozygous109049772
1142104556142104556TT53GENIChomozygous130823695
1142089543142089543CTTT22GENIChomozygous130823693
1142095924142095924A54GENIChomozygous130823694