chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34060104640601047GA61GENICpossibly homozygous779526898
34060146140601462CT89GENICheterozygous779526899
34060147840601479CT96GENICheterozygous779526900
34060149640601497GT99GENICheterozygous779526901
34060150240601503GA100GENICheterozygous779526902
34060150540601506CT98GENICheterozygous779526903
34060155540601556GA77GENICheterozygous779526904
34060155940601560GT77GENICheterozygous779526905
34060156240601563GA77GENICheterozygous779526906
34060157040601571GA76GENICheterozygous779526907
34060157340601574GA72GENICheterozygous779526908
34060157740601578TG71GENICheterozygous779526909
34060178840601789AC67GENICheterozygous779526910
34060179440601795CT74GENICheterozygous779526911
34060180240601803CT77GENICheterozygous779526912
34060185240601853CT78GENICheterozygous779526913
34060185340601854CG76GENICheterozygous779526914
34060190740601908TC83GENICheterozygous779526915
34060192540601926TC81GENICheterozygous779526916
34060194640601947GA85GENICheterozygous779526917
34060194840601949GA84GENICheterozygous779526918
34060196140601962TC80GENICheterozygous779526919
34060197240601973CT75GENICheterozygous779526920
34060197740601978AG75GENICheterozygous779526921
34060198240601983GA73GENICheterozygous779526922
34060199340601994TC75GENICheterozygous779526923
34060199440601995GA77GENICheterozygous779526924
34060266940602670GA45GENIChomozygous779526925
34060267940602680AG44GENICpossibly homozygous779526926
34060269640602697AG37GENIChomozygous779526927
34060269740602698AC37GENIChomozygous779526928
34060272440602725CG34GENIChomozygous779526929
34060272740602728CA34GENICpossibly homozygous779526930
34060275940602760TG34GENIChomozygous779526931
34060303540603036CT51GENICpossibly homozygous779526932