chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263449011263449012GT8GENIChomozygous109027024
1263449595263449596TA13GENIChomozygous109027025
1263450387263450388AG17GENIChomozygous108633075
1263451566263451567AG11GENIChomozygous109027026
1263453135263453136AG17GENIChomozygous108633083
1263453906263453907GA18GENIChomozygous109217063
1263455588263455589AT14GENIChomozygous108633087
1263456989263456990AC4GENIChomozygous120734039
1263456991263456992CT3GENIChomozygous120734041
1263456993263456994CG2GENIChomozygous120734043
1263459229263459230GA8GENIChomozygous108633095
1263459234263459235GC8GENIChomozygous108633097
1263459683263459684TC12GENIChomozygous109217072
1263461149263461150AC15GENIChomozygous109217076
1263461176263461177TC12GENIChomozygous109217078
1263461297263461298AG16GENIChomozygous108633113
1263463247263463248CT19GENIChomozygous109217080
1263463258263463259CT17GENIChomozygous108633116
1263466238263466239TC12GENIChomozygous109217084
1263466353263466354GA9GENIChomozygous109217086
1263466568263466569CT15GENIChomozygous108633118
1263466863263466864AG18GENIChomozygous108633120
1263466864263466865GT19GENIChomozygous108633122
1263466987263466988TG12GENIChomozygous108633124
1263467003263467004CT12GENIChomozygous108633126
1263467041263467042CG13GENIChomozygous108633128
1263467593263467594AG14GENIChomozygous108633130
1263467846263467847CT13GENIChomozygous108633132
1263469726263469727GA12GENIChomozygous108633154
1263469762263469763AG12GENIChomozygous108633156
1263469790263469791GA10GENIChomozygous108633158
1263469803263469804GA9GENIChomozygous108633160
1263469905263469906CG15GENIChomozygous108633162
1263470132263470133GC11GENIChomozygous108633164
1263470138263470139TC11GENIChomozygous108633166
1263470449263470450CT13GENIChomozygous108633168
1263470464263470465CT16GENIChomozygous108633170
1263470531263470532TC23GENIChomozygous108633172
1263470736263470737TC19GENIChomozygous108633174
1263472263263472264CT19GENIChomozygous108633178