chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1168549218168549219AG28GENIChomozygous60936121
1168549613168549614TC18GENIChomozygous60936122
1168549624168549626AA--8GENICheterozygous60936123
1168549625168549626A-8GENICheterozygous60936124
1168550320168550321GGT25GENIChomozygous60936125
1168550414168550415AG30GENIChomozygous60936126
1168550970168550971GC21GENIChomozygous60936127
1168551054168551055AG17GENIChomozygous60936128
1168551137168551139GG--14GENICpossibly homozygous60936131
1168551140168551141GA15GENICpossibly homozygous61552830
1168551175168551176AC28GENICheterozygous60936132
1168551330168551331TC21GENIChomozygous60936134
1168551788168551789TC24GENIChomozygous60936135
1168551822168551823TC18GENIChomozygous60936136
1168552120168552121AG30GENIChomozygous60936137
1168552358168552359TC20GENIChomozygous60936138
1168552424168552425AG18GENIChomozygous60936139
1168552573168552574AG17GENIChomozygous60936140
1168553077168553083AAAAAA------4GENIChomozygous60936141
1168553105168553106A-1GENIChomozygous60936142
1168553622168553623GA22GENIChomozygous60936143
1168553751168553752AG22GENIChomozygous60936144
1168553924168553925CT15GENIChomozygous60936145
1168553934168553935CT20GENIChomozygous60936146
1168554101168554102AAT26GENIChomozygous60936147
1168554397168554398AAT15GENIChomozygous60936148
1168554833168554834TTGTGA31GENIChomozygous60936149
1168555250168555251CCAAAG19GENIChomozygous60936150
1168555460168555461GA27GENIChomozygous61552831
1168555502168555503CT37GENICheterozygous60936151
1168555766168555767GA21GENIChomozygous60936156
1168555557168555558GA29GENIChomozygous60936153
1168555650168555651TC25GENIChomozygous60936154
1168555688168555689A-19GENIChomozygous60936155
1168556125168556126TC26GENIChomozygous61552832
1168556489168556490TG24GENIChomozygous61552833
1168556567168556568AG15GENIChomozygous61552834
1168556852168556853GC20GENIChomozygous60936166
1168565873168565874GT24GENICheterozygous61552835