chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8110604182110604183CA14GENIChomozygous52802111
8110604482110604483CG12GENIChomozygous52802113
8110604804110604805AG19GENIChomozygous52802115
8110604922110604923AC20GENIChomozygous52802117
8110605131110605132CT22GENIChomozygous52802119
8110605180110605181CT21GENIChomozygous52802121
8110605702110605703TC27GENIChomozygous52802123
8110606000110606001CT31GENIChomozygous52802125
8110606444110606446CA--5GENIChomozygous53522508
8110607345110607346GA25GENIChomozygous52802129
8110607608110607609CCTTTTTTTTTTTT12GENICheterozygous53579682
8110607973110607974GGTTTT27GENIChomozygous52802130
8110608350110608354GTGT----15GENICheterozygous52802134
8110608352110608354GT--15GENICheterozygous52802136
8110609470110609471AAG18GENIChomozygous52802138
8110609478110609479GT18GENIChomozygous52802140
8110610613110610614GGCACACACACACACA1GENIChomozygous53522512
8110612611110612612GA18GENIChomozygous52802142
8110613628110613629TTC12GENIChomozygous52802144
8110614033110614034GA20GENIChomozygous53164394
8110614289110614290AG15GENIChomozygous52802146
8110614667110614668AG28GENIChomozygous52802148
8110614837110614838CT32GENIChomozygous52802150
8110614881110614882CG35GENIChomozygous52802152
8110614884110614885AG35GENIChomozygous52802154
8110615410110615411GGC12GENIChomozygous52802156
8110615905110615906GC34GENIChomozygous52802158
8110616387110616388TC42GENIChomozygous52802160