chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108957757089577571CT28GENIChomozygous117087624
108957761989577620TG23GENIChomozygous117087626
108957766989577670TC22GENIChomozygous117087628
108957795289577953AC11GENIChomozygous116820349
108957795889577959CT9GENIChomozygous117087630
108957814289578143GA14GENIChomozygous117087632
108957818289578183GT15GENICpossibly homozygous117087634
108957847989578480TG22GENIChomozygous117087636
108957874389578744CG23GENIChomozygous116820351
108957891489578915GA14GENIChomozygous117087638
108957914189579142AC13GENIChomozygous116820353
108957936089579361GC35GENIChomozygous117087640