chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7134627479134627480GA17GENIChomozygous138230353
7134628778134628779AG23GENIChomozygous138230354
7134629505134629506TG27GENIChomozygous138230355
7134630119134630120CA17GENICpossibly homozygous138230356
7134630266134630267CT18GENIChomozygous138230357
7134630598134630599TC26GENIChomozygous138230358
7134631237134631238TG17GENIChomozygous138230359
7134631241134631242TC16GENIChomozygous138230360
7134631261134631262CG16GENIChomozygous138230361
7134631394134631395GT18GENIChomozygous138230362
7134631521134631522GA25GENIChomozygous138230363
7134633169134633170AT21GENIChomozygous138230364
7134633602134633603AG17GENIChomozygous138230365
7134634272134634273GA18GENIChomozygous138230366
7134635216134635217AG26GENIChomozygous138230367
7134635302134635303GA24GENIChomozygous138230368
7134635865134635866GA21GENIChomozygous138230369
7134638039134638040TC6GENIChomozygous138230371
7134638594134638595AG15GENIChomozygous138230372
7134640388134640389GA19GENIChomozygous138230373
7134640855134640856GA18GENIChomozygous138230374
7134642132134642133GT14GENIChomozygous138230375
7134643822134643823GA21GENIChomozygous138230376
7134644325134644326GA24GENIChomozygous138230377
7134638457134638462TTTTG8GENIChomozygous137985587
7134639892134639893T14GENIChomozygous137985588
7134642940134642940AG14GENIChomozygous137985590
7134642424134642424TTTTC6GENICheterozygous140893201
7134653114134653115CT25GENIChomozygous138230378
7134641848134641849AG6GENICheterozygous403896442
7134639892134639893TC14GENICheterozygous403228296
7134641848134641849A6GENIChomozygous403896441