chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
112418172624181727GA11GENIChomozygous935907436
112418279024182791GA27GENICpossibly homozygous935907437
112418400424184005GT31GENIChomozygous935907438
112418400724184008TG31GENIChomozygous935907439
112418445924184460CA29GENIChomozygous935907440
112418490724184908AG14GENIChomozygous935907441
112418531824185319CA18GENIChomozygous935907442
112418567024185671TC18GENIChomozygous935907443
112418668324186684AT23GENIChomozygous935907444
112418684124186842GA12GENIChomozygous935907445
112418693024186931CT23GENIChomozygous935907446
112418718524187186AC17GENIChomozygous935907447
112418761624187617CT32GENIChomozygous935907448
112418796924187970CT25GENIChomozygous935907449
112418816124188162GA22GENIChomozygous935907450
112418968824189689TC24GENIChomozygous935907451
112419055224190553CT29GENIChomozygous935907452
112419055524190556GA24GENIChomozygous935907453
112419071024190711AT26GENIChomozygous935907454
112419282224192823CT13GENIChomozygous935907455