chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1168549218168549219AG22GENIChomozygous60936121
1168549613168549614TC13GENIChomozygous60936122
1168549625168549626A-2GENICheterozygous60936124
1168550320168550321GGT15GENIChomozygous60936125
1168550414168550415AG23GENIChomozygous60936126
1168550970168550971GC22GENIChomozygous60936127
1168551054168551055AG21GENIChomozygous60936128
1168551140168551141GA7GENIChomozygous61552830
1168551330168551331TC21GENIChomozygous60936134
1168551788168551789TC23GENIChomozygous60936135
1168551822168551823TC33GENICpossibly homozygous60936136
1168552120168552121AG21GENIChomozygous60936137
1168552358168552359TC27GENIChomozygous60936138
1168552424168552425AG19GENIChomozygous60936139
1168552573168552574AG13GENIChomozygous60936140
1168553077168553083AAAAAA------4GENICheterozygous60936141
1168553080168553083AAA---4GENICheterozygous62369173
1168553104168553105G-8GENICheterozygous62172287
1168553105168553106A-8GENICheterozygous60936142
1168553622168553623GA22GENIChomozygous60936143
1168553751168553752AG19GENIChomozygous60936144
1168553924168553925CT17GENIChomozygous60936145
1168553934168553935CT15GENIChomozygous60936146
1168554101168554102AAT27GENIChomozygous60936147
1168554397168554398AAT17GENIChomozygous60936148
1168554833168554834TTGTGA33GENIChomozygous60936149
1168555250168555251CCAAAG23GENICpossibly homozygous60936150
1168555460168555461GA15GENIChomozygous61552831
1168555481168555482TTTTGGTTGGTTGGTTGG8GENIChomozygous62172289
1168555557168555558GA21GENIChomozygous60936153
1168555650168555651TC27GENIChomozygous60936154
1168555688168555689A-31GENIChomozygous60936155
1168555766168555767GA38GENIChomozygous60936156
1168556125168556126TC25GENIChomozygous61552832
1168556489168556490TG29GENIChomozygous61552833
1168556567168556568AG21GENIChomozygous61552834
1168556852168556853GC14GENIChomozygous60936166