chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8103793083103793083T14GENIChomozygous138261507
8103794199103794200GA18GENIChomozygous138401526
8103795700103795701TC13GENIChomozygous138401527
8103795785103795786TC19GENIChomozygous138401528
8103797494103797495GA20GENIChomozygous138401529
8103801196103801196A14GENICpossibly homozygous138261508
8103801378103801379GA20GENIChomozygous138401530
8103801444103801445GA26GENIChomozygous138401531
8103801471103801472GA21GENIChomozygous138401532
8103802162103802163CT23GENIChomozygous138401533
8103803389103803390GA22GENIChomozygous138401534
8103803691103803692TC19GENIChomozygous138401535
8103804382103804383GC17GENIChomozygous138401536
8103804586103804587GA22GENIChomozygous138401537
8103805717103805718AT22GENIChomozygous138401538
8103806972103806973GT22GENIChomozygous138401539
8103807111103807111CTAGCGCAGAGG9GENIChomozygous138261509
8103808499103808501AG16GENIChomozygous138261510
8103808523103808524TC15GENIChomozygous138401540
8103809185103809186AG16GENIChomozygous138401541
8103809803103809804AG7GENIChomozygous138401542
8103811486103811487TG14GENIChomozygous138401543
8103812695103812696A15GENIChomozygous138261511
8103812848103812849GA18GENIChomozygous138401544
8103813640103813641A9GENIChomozygous138261512
8103813750103813751GA5GENIChomozygous138401545
8103815097103815098AG25GENIChomozygous138401546
8103815326103815327GA17GENIChomozygous138401547
8103816039103816040CT13GENIChomozygous138401548
8103816191103816192TC18GENIChomozygous138401549
8103807244103807245AT7GENICheterozygous403247357
8103806047103806048CT16GENICheterozygous154553845
8103813640103813641AG9GENICheterozygous154553847
8103806047103806048C16GENIChomozygous403247355
8103807244103807245A7GENICheterozygous403247356