chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125743664125743669GCATA-----14GENICpossibly homozygous726056621
7125744277125744278AC29GENIChomozygous594284535
7125744898125744899GA23GENIChomozygous594284536
7125745046125745047TA19GENIChomozygous594284537
7125745150125745151AT25GENIChomozygous594284538
7125745567125745568TTTG7GENIChomozygous726056622
7125745717125745718GT30GENIChomozygous594284539
7125745937125745938GA30GENIChomozygous594284540
7125746484125746485AG32GENIChomozygous594284541
7125746618125746619GA32GENIChomozygous594284542
7125747534125747535CT30GENIChomozygous593752607
7125747571125747572GA41GENIChomozygous593752608
7125748329125748330AG33GENIChomozygous593752609
7125748832125748833C-12GENIChomozygous726056623
7125748927125748928GA53GENIChomozygous593752610
7125749012125749013GA36GENIChomozygous593752611
7125749414125749415AG25GENIChomozygous593752612
7125749466125749467TTG27GENIChomozygous726056624
7125751521125751522AAT16GENICheterozygous726056625
7125751521125751522AATT16GENICheterozygous726056626
7125752000125752001TC30GENIChomozygous593752613
7125752756125752757GA30GENIChomozygous593752614
7125753821125753822CT24GENIChomozygous594284543
7125753897125753898CT26GENIChomozygous593752615
7125753949125753950GA30GENIChomozygous593752616
7125754274125754275AG30GENIChomozygous593752617
7125754320125754321CT33GENIChomozygous593752618
7125754367125754368CT30GENIChomozygous593752619
7125754379125754380GC29GENIChomozygous593752620
7125755157125755158GA21GENIChomozygous593752621
7125755666125755667CT31GENIChomozygous593752622
7125755703125755704CT28GENIChomozygous593752623
7125756500125756501TC25GENIChomozygous593752624
7125756849125756850AG25GENIChomozygous593752625
7125756965125756966GGAAAA13GENICheterozygous726056628
7125756965125756966GGAAAAAAAAAAA13GENICheterozygous726056629
7125757153125757154TTA20GENICpossibly homozygous726056630
7125757153125757154TTAA20GENICheterozygous726056631