chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34060104640601047GA45GENIChomozygous793257071
34060146140601462CT50GENICheterozygous793257072
34060147840601479CT59GENICheterozygous793257073
34060149640601497GT62GENICheterozygous793257074
34060150240601503GA61GENICheterozygous793257075
34060150540601506CT61GENICheterozygous793257076
34060155540601556GA56GENICheterozygous793257077
34060155940601560GT56GENICheterozygous793257078
34060156240601563GA54GENICheterozygous793257079
34060157740601578TG53GENICheterozygous793257080
34060175640601757CT42GENICheterozygous793257081
34060175840601759AG41GENICheterozygous793257082
34060176640601767CT44GENICheterozygous793257083
34060177040601771TC47GENICheterozygous793257084
34060178840601789AC53GENICheterozygous793257085
34060179440601795CT55GENICheterozygous793257086
34060180240601803CT50GENICheterozygous793257087
34060185240601853CT54GENICheterozygous793257088
34060185340601854CG52GENICheterozygous793257089
34060190740601908TC64GENICheterozygous793257090
34060192540601926TC61GENICheterozygous793257091
34060194640601947GA56GENICheterozygous793257092
34060194840601949GA57GENICheterozygous793257093
34060196140601962TC64GENICheterozygous793257094
34060197240601973CT70GENICheterozygous793257095
34060197740601978AG69GENICheterozygous793257096
34060198240601983GA65GENICheterozygous793257097
34060199340601994TC58GENICheterozygous793257098
34060199440601995GA55GENICheterozygous793257099
34060266940602670GA21GENIChomozygous793257100
34060267940602680AG22GENIChomozygous793257101
34060269640602697AG22GENIChomozygous793257102
34060269740602698AC22GENIChomozygous793257103
34060272440602725CG17GENIChomozygous793257104
34060272740602728CA18GENIChomozygous793257105
34060275940602760TG17GENIChomozygous793257106
34060303540603036CT36GENICpossibly homozygous793257107