chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2165612451165612452GA6GENIChomozygous120209156
2165612897165612898AG32GENIChomozygous110113168
2165613554165613555GA26GENIChomozygous110113169
2165613753165613754GA31GENIChomozygous110113170
2165614541165614542GA28GENIChomozygous120209157
2165614628165614629GC27GENIChomozygous120209158
2165615677165615678AG26GENIChomozygous120209159
2165616444165616445GA29GENIChomozygous120209160
2165616447165616448CT29GENIChomozygous120209161
2165617548165617549AG24GENIChomozygous110113172
2165617598165617599AC27GENIChomozygous110113173
2165617770165617771TG34GENIChomozygous110896059
2165618140165618141TC25GENIChomozygous120209162
2165618461165618462CT16GENIChomozygous120375701
2165618713165618714GA19GENIChomozygous110113175
2165618764165618765GA11GENIChomozygous120209163
2165619484165619485TC30GENIChomozygous120209164
2165619724165619725GA23GENIChomozygous110113179
2165620403165620404GC28GENIChomozygous120209165
2165621972165621973GT32GENICpossibly homozygous120209166
2165622119165622120AG28GENIChomozygous120209167
2165625462165625463GA21GENIChomozygous120209168
2165625863165625864AT11GENIChomozygous120128290
2165626518165626519AG31GENIChomozygous110113192
2165626916165626917TC34GENIChomozygous120209169
2165627172165627173CG31GENIChomozygous110113194