chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2283479779283479780CA6GENIChomozygous59617363
2283481899283481903AAGG----11GENICpossibly homozygous59617365
2283481936283481937GA19GENICpossibly homozygous59617371
2283483498283483499TC22GENIChomozygous59617373
2283483790283483791GA40GENIChomozygous59617375
2283483866283483867AG52GENIChomozygous59617377
2283484582283484583AT18GENIChomozygous59617379
2283484762283484764TA--28GENIChomozygous59617381
2283484878283484879AG29GENIChomozygous59617383
2283484958283484959C-26GENIChomozygous59617385
2283487247283487248A-12GENICheterozygous60564217
2283488430283488431TC33GENICpossibly homozygous59617387
2283493307283493311AAAA----13GENICpossibly homozygous59617389
2283493308283493311AAA---13GENICheterozygous59617391
2283493864283493865AAT18GENIChomozygous59617393
2283494030283494031GGAAAAC19GENIChomozygous59617395
2283494313283494314AAT17GENICpossibly homozygous59617397
2283497587283497588TC16GENIChomozygous59617399
2283497657283497658A-18GENIChomozygous59617403
2283498119283498120AT35GENIChomozygous59617407
2283498827283498828TC10GENIChomozygous59617409
2283499132283499134AA--7GENIChomozygous59782660
2283501173283501174GC10GENIChomozygous59617411
2283501278283501279CCTT11GENIChomozygous59617413
2283503972283503973CT24GENIChomozygous59617415
2283498859283498860GGA7GENICheterozygous60830028