chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142203513142203514AC39GENIChomozygous116097634
7142204642142204643AG28GENIChomozygous115941537
7142204974142204975TC23GENIChomozygous115941538
7142205990142205991TC28GENIChomozygous115941539
7142208176142208177GC28GENIChomozygous116097636
7142211327142211328GT16GENIChomozygous116097640
7142215212142215213TA20GENIChomozygous116097642
7142217149142217150AG40GENIChomozygous115941543
7142217582142217583TC42GENIChomozygous115941549
7142218160142218161AG19GENIChomozygous115941553
7142220473142220474TC34GENIChomozygous116097648
7142221392142221393AG22GENIChomozygous115941555
7142221697142221698AC37GENIChomozygous115941556
7142221796142221797GA43GENIChomozygous116097650
7142222008142222009TC35GENICpossibly homozygous115941557
7142223300142223301TA19GENIChomozygous115941563