chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125746090125746091CT38GENIChomozygous628397318
7125747342125747343CT25GENIChomozygous628397319
7125747534125747535CT25GENIChomozygous628397320
7125747571125747572GA31GENIChomozygous628397321
7125748329125748330AG24GENIChomozygous628397322
7125748832125748833C-2GENIChomozygous744524068
7125748927125748928GA35GENIChomozygous628397323
7125749012125749013GA18GENIChomozygous628397324
7125749414125749415AG19GENIChomozygous628397325
7125751521125751522AAT10GENICheterozygous744524069
7125751521125751522AATT10GENICheterozygous744524070
7125752000125752001TC23GENIChomozygous628397326
7125752756125752757GA14GENIChomozygous628397327
7125753821125753822CT14GENIChomozygous628397328
7125753897125753898CT25GENIChomozygous628397329
7125753949125753950GA20GENIChomozygous628397330
7125754274125754275AG27GENIChomozygous628397331
7125754320125754321CT23GENIChomozygous628397332
7125754367125754368CT16GENIChomozygous628397333
7125754379125754380GC19GENIChomozygous628397334
7125755157125755158GA15GENICpossibly homozygous628397335
7125755666125755667CT20GENIChomozygous628397336
7125755703125755704CT22GENIChomozygous628397337
7125756500125756501TC19GENIChomozygous628397338
7125756849125756850AG18GENIChomozygous628397339
7125756965125756966GGA10GENICheterozygous744524071
7125756965125756966GGAAAA10GENICheterozygous744524072
7125756965125756966GGAAAAAAAAAAA10GENICheterozygous744524073
7125757153125757154TTA19GENICpossibly homozygous744524074