chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5146849850146849851CCAAA7GENIChomozygous55774066
5146850189146850193TTTT----21GENIChomozygous55774068
5146851882146851883AAT32GENIChomozygous55774070
5146852721146852722T-17GENIChomozygous55774072
5146852734146852735GGT14GENIChomozygous55774074
5146852968146852969CT46GENIChomozygous55774076
5146853406146853407TC58GENIChomozygous55774078
5146853515146853516GA43GENIChomozygous55774080
5146855740146855741GA58GENIChomozygous55774082
5146856026146856028TT--19GENICheterozygous55774084
5146856027146856028T-19GENICpossibly homozygous55774086
5146856158146856159AC23GENIChomozygous55774088
5146856359146856360GA7GENIChomozygous55774089
5146859139146859140CCT11GENICheterozygous55774091
5146859272146859273CT37GENIChomozygous55774093
5146859278146859279TC38GENIChomozygous55774095
5146859967146859968A-1GENIChomozygous55774097
5146860034146860035GA48GENIChomozygous55774099
5146860218146860219GA31GENIChomozygous55774101
5146860221146860222AAACAGGACTT28GENIChomozygous55774103
5146860248146860249TC41GENIChomozygous55774105
5146861052146861053CCTT1GENIChomozygous55774107
5146861182146861183TA19GENICheterozygous55774109
5146861185146861186GA19GENICheterozygous55774111
5146862027146862028G-49GENIChomozygous55774113
5146862310146862311GA24GENICpossibly homozygous55774115
5146863669146863670CT47GENICheterozygous55774117
5146864100146864101TG23GENICheterozygous55774119
5146865673146865674CT41GENICheterozygous55774121
5146867365146867374CAGCTCTCA---------11GENIChomozygous55774123
5146867742146867743AAAAAC31GENIChomozygous55774125
5146869351146869352GA43GENICpossibly homozygous55774127
5146869394146869398CTCG----44GENIChomozygous55774129