chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85090719550907196AG29GENIChomozygous138329605
85090775350907753C33GENIChomozygous138244842
85091211650912117TC45GENIChomozygous138329609
85090853050908531AC61GENIChomozygous138329606
85091077050910771AG49GENIChomozygous138329607
85091093150910932AG62GENIChomozygous138329608
85091333550913340CTGGT39GENIChomozygous138244843
85091346850913469AT45GENIChomozygous138329610
85091348450913485GA43GENIChomozygous138329611
85091352350913530CTTTATC47GENIChomozygous138244844
85091469650914697GA49GENIChomozygous138329612
85091471750914718GA51GENIChomozygous138329613
85091666850916669A52GENIChomozygous138244845
85091704450917045CT44GENIChomozygous138329614
85091849250918493GA54GENIChomozygous138329615
85091883750918838CT45GENIChomozygous138329616
85092284350922844GA53GENIChomozygous138329617
85092286050922861AG51GENIChomozygous138329618
85092405050924056AGACAG38GENIChomozygous138244846
85092479450924796TT42GENIChomozygous138244847
85092489250924893CT55GENIChomozygous138329619
85092546550925466AG49GENIChomozygous138329620
85092709150927092AG41GENIChomozygous138329621
85092712350927124AG41GENIChomozygous138329622
85092817550928176TC18GENIChomozygous138329623
85092849350928494AG20GENIChomozygous138329624
85092857150928572AC25GENIChomozygous138329625
85092858450928589AGGGC23GENIChomozygous138244848
85092949050929491CT16GENIChomozygous138329626
85091528850915289G33GENICpossibly homozygous403237539
85091528850915289GA33GENICheterozygous154517078
85092695750926958T32GENIChomozygous403237540
85092695750926958TC32GENICheterozygous403237541
85093071750930718TC51GENIChomozygous138329627
85093074350930744GA45GENIChomozygous138329628
85093097550930976CA46GENIChomozygous138329629
85093203250932032GT25GENIChomozygous138244849
85093206150932062CT25GENIChomozygous138329630
85093209650932097GA27GENIChomozygous404196651
85093209650932097G27GENICheterozygous404196652
85092289050922891TA56GENIChomozygous144394923