chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159590044159590045CT16GENIChomozygous985234967
5159590355159590356AC15GENIChomozygous985234968
5159590356159590357GC15GENIChomozygous985234969
5159590377159590378GA17GENIChomozygous985234970
5159590516159590517AG11GENIChomozygous985234971
5159590543159590544TC6GENIChomozygous985234972
5159590567159590568TC5GENIChomozygous985234973
5159590810159590811GA6GENIChomozygous985234974
5159591041159591042CT13GENIChomozygous985234975
5159591165159591166AG16GENIChomozygous985234976
5159591294159591295GA32GENIChomozygous985234977
5159591492159591493CT17GENIChomozygous985234978
5159591711159591712GA12GENIChomozygous985234979
5159591959159591960CT9GENIChomozygous985234980
5159592241159592242AG16GENIChomozygous985234981
5159592551159592552GA14GENIChomozygous985234982
5159592713159592714CT20GENIChomozygous985234983
5159593011159593012TA22GENIChomozygous985234984
5159593229159593230AG15GENIChomozygous985234985
5159593316159593317AC10GENIChomozygous985234986
5159594481159594482GA12GENIChomozygous985234987
5159595521159595522GA18GENIChomozygous985234988
5159598268159598269GA14GENIChomozygous985234989
5159599504159599505TC13GENIChomozygous985234990
5159601143159601144CT19GENIChomozygous985234991
5159601217159601218AG11GENIChomozygous985234992
5159601274159601275AG20GENIChomozygous985234993
5159602018159602019CT2GENIChomozygous985234994