chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18027358980273590AG11GENIChomozygous109298504
18027420780274208TC15GENIChomozygous120868287
18027628480276285AG20GENIChomozygous109298506
18027731280277313GA10GENIChomozygous120868288
18027797480277975AG6GENIChomozygous109298510
18027876780278768TC15GENIChomozygous109298514
18027962380279624TC7GENIChomozygous109298518
18028286680282867GT5GENIChomozygous120868289
18028359980283600CT8GENIChomozygous120868290
18028374180283742CT13GENIChomozygous120868291
18028387780283878AC27GENIChomozygous109298528
18028422280284223AG18GENIChomozygous120481174
18028424780284248AG22GENIChomozygous120868292
18028471280284713CG6GENIChomozygous120481175
18028507580285076AG13GENIChomozygous120868293
18028513780285138GA9GENIChomozygous109298535
18028517280285173CT11GENIChomozygous120868294
18028518980285190CT12GENIChomozygous120868295
18028536580285366TA16GENIChomozygous120868296
18028539280285393AG18GENIChomozygous109298537
18028553980285540AG12GENIChomozygous120868297
18028562380285624GA11GENIChomozygous120868298
18028576280285763TA33GENIChomozygous120868299
18028622180286222TC34GENIChomozygous120868300
18028635680286357CG24GENIChomozygous120868301
18028639780286398TG20GENICpossibly homozygous120868302
18028639980286400AG20GENICpossibly homozygous120868303
18028647580286476GC22GENICpossibly homozygous109298543
18028697580286976GA14GENIChomozygous120868304
18028699480286995GC11GENIChomozygous120868305
18028707580287076AG9GENIChomozygous109298547
18028804180288042GA7GENIChomozygous109298551
18029010880290109CT19GENIChomozygous120868306
18029033980290340TC18GENIChomozygous109298553
18029078580290786GA16GENIChomozygous120868307