chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142202712142202713AG47GENICpossibly homozygous115941536
7142203513142203514AC60GENIChomozygous116097634
7142204642142204643AG34GENIChomozygous115941537
7142204974142204975TC49GENIChomozygous115941538
7142205990142205991TC40GENIChomozygous115941539
7142208176142208177GC37GENIChomozygous116097636
7142209559142209560TC32GENICpossibly homozygous116350252
7142211327142211328GT30GENICpossibly homozygous116097640
7142215212142215213TA63GENIChomozygous116097642
7142217149142217150AG56GENIChomozygous115941543
7142217582142217583TC66GENICpossibly homozygous115941549
7142217629142217630TG82GENICheterozygous115941550
7142217641142217642AG70GENICheterozygous115941551
7142217657142217658GC80GENICheterozygous116097644
7142217660142217661TA80GENICheterozygous116097646
7142218160142218161AG52GENIChomozygous115941553
7142220236142220237GA7GENIChomozygous116265495
7142220473142220474TC45GENIChomozygous116097648
7142221392142221393AG32GENICpossibly homozygous115941555
7142221697142221698AC51GENIChomozygous115941556
7142221796142221797GA51GENIChomozygous116097650
7142222008142222009TC47GENIChomozygous115941557
7142223015142223016CT49GENICheterozygous116305369
7142223027142223028CT51GENICheterozygous116305370
7142223039142223040CT51GENICheterozygous116305371
7142223051142223052CT50GENICheterozygous116305372
7142223300142223301TA45GENICpossibly homozygous115941563