chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
38089318480893185TC12GENIChomozygous111635909
38089319880893199GT8GENIChomozygous111635910
38089465780894658TG16GENIChomozygous111635913
38089485880894859TC11GENIChomozygous111635914
38089487180894872TC13GENIChomozygous111635915
38089599080895991GA22GENIChomozygous111635916
38089714080897141TC24GENIChomozygous111635917
38089759180897592AT19GENIChomozygous111635918
38090683880906839TC21GENIChomozygous111635921
38090736080907361CT39GENICheterozygous111635922
38090868580908686AG25GENIChomozygous111635923
38090886680908867CA22GENICheterozygous111635924
38090900680909007CT25GENICpossibly homozygous111635925
38090996980909970GA23GENIChomozygous111635926
38091468880914689AT29GENIChomozygous111635927
38091530280915303GA32GENIChomozygous111635928
38091959980919600AG8GENIChomozygous111635929
38092327980923280CG24GENIChomozygous111635930
38093077480930775CT18GENIChomozygous111635931
38093123380931234CT21GENIChomozygous111635932