chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1142087849142087850AG30GENIChomozygous109049763
1142088675142088676C25GENICpossibly homozygous130520089
1142089543142089543CTTT8GENIChomozygous130823693
1142091637142091638GA30GENIChomozygous108937351
1142095924142095924A18GENIChomozygous130823694
1142096564142096565GT27GENIChomozygous109049765
1142092365142092366T32GENICpossibly homozygous127439686
1142095281142095282AG24GENIChomozygous108262659
1142097858142097859GT7GENIChomozygous108262661
1142089696142089697CT15GENICheterozygous132001970
1142104556142104556TT21GENIChomozygous130823695
1142105585142105586GA28GENIChomozygous109049772
1142100410142100411TG26GENIChomozygous108262663
1142100485142100486TC36GENIChomozygous109327838
1142100490142100491AC34GENIChomozygous109049770
1142101397142101398GC14GENIChomozygous109049771
1142104770142104771TC29GENIChomozygous108262665
1142098430142098431TG10GENIChomozygous108743914
1142098434142098435TG10GENIChomozygous108743916