chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4138865102138865102TATAGGAAGGAGATTCATAATTATAGCCAA26GENIChomozygous128083955
4138865125138865127CT22GENIChomozygous128083956
4138866075138866076AG25GENIChomozygous112850922
4138866886138866887A28GENIChomozygous128083957
4138867636138867637GA28GENIChomozygous112850926
4138868001138868001TTA22GENIChomozygous128083958
4138870835138870836GT24GENIChomozygous112850928
4138871079138871080GT23GENIChomozygous112850930
4138871400138871401AC30GENIChomozygous112850932
4138872697138872698TC26GENIChomozygous112850934
4138872978138872979TC26GENIChomozygous112850936
4138873825138873830GAAAA20GENIChomozygous128083959
4138874154138874155TC26GENIChomozygous112850938
4138874430138874433CAC8GENIChomozygous128083960
4138874448138874448CT9GENIChomozygous128083961
4138875086138875087TA24GENIChomozygous112850940
4138875208138875209AT22GENIChomozygous112850942
4138875676138875676A17GENICpossibly homozygous128083962
4138876322138876323TC16GENIChomozygous112850944
4138877302138877303T13GENIChomozygous128083963
4138879503138879504GA23GENIChomozygous112850946
4138882652138882653CA22GENIChomozygous112850948
4138883541138883543TG18GENIChomozygous128083964
4138884569138884570TC29GENIChomozygous112850950
4138883543138883544TC18GENIChomozygous119281149
4138879978138879979CA25GENIChomozygous113055356
4138877913138877914T16GENICheterozygous130938064