chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
589114168911417GT10GENIChomozygous113639405
589118048911805TC25GENIChomozygous119139946
589158748915875AG31GENIChomozygous113639419
589161238916124GA40GENIChomozygous119139948
589163808916381CT19GENIChomozygous119139950
589166328916633TC25GENIChomozygous113639433
589184798918480AC24GENIChomozygous119139952
589187048918705AC26GENIChomozygous113639438
589194758919476AG20GENIChomozygous113639444
589203408920341CT32GENIChomozygous113639450
589206528920653TG27GENIChomozygous113639452
589216428921643AG30GENIChomozygous113639458
589178058917806CT5GENIChomozygous119200882
589252418925242CA20GENIChomozygous113639557
589301808930181AG25GENIChomozygous113639608
589365638936564AG18GENIChomozygous119139956
589401238940124AG21GENIChomozygous119139962
589426098942610TC9GENIChomozygous119139964
589453668945367AG29GENIChomozygous119139966
589461088946109TC28GENIChomozygous114170320
589467508946751TC24GENIChomozygous119139968
589487518948752AG18GENIChomozygous113639652
589489938948994AG19GENIChomozygous113639654
589492828949283GA27GENIChomozygous113639656
589499148949915AG17GENIChomozygous113639658
589503998950400CT29GENIChomozygous119139970
589506188950619CT22GENIChomozygous119139972
589506408950641GA21GENIChomozygous119139974
589511728951173TC16GENIChomozygous114170328
589538098953810AT19GENIChomozygous113639664
589543798954380CG32GENIChomozygous119139976
589555628955563AG30GENIChomozygous113639667
589556128955613GT25GENIChomozygous113639669