chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142202712142202713AG5GENIChomozygous115941536
7142203513142203514AC5GENIChomozygous116097634
7142204642142204643AG12GENIChomozygous115941537
7142204974142204975TC12GENIChomozygous115941538
7142205990142205991TC23GENIChomozygous115941539
7142208176142208177GC24GENIChomozygous116097636
7142211327142211328GT19GENIChomozygous116097640
7142215212142215213TA20GENIChomozygous116097642
7142217149142217150AG28GENICheterozygous115941543
7142217492142217493CT5GENICheterozygous126620931
7142217582142217583TC19GENICheterozygous115941549
7142218160142218161AG5GENIChomozygous115941553
7142220473142220474TC9GENIChomozygous116097648
7142221392142221393AG18GENIChomozygous115941555
7142221697142221698AC16GENIChomozygous115941556
7142221796142221797GA14GENIChomozygous116097650
7142222008142222009TC12GENIChomozygous115941557
7142223300142223301TA17GENIChomozygous115941563
7142209559142209560TC6GENIChomozygous116350252
7142217398142217399AT8GENICheterozygous126588107
7142217246142217247GA7GENICheterozygous126660148