chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7134627479134627480GA49GENIChomozygous138230353
7134628778134628779AG52GENIChomozygous138230354
7134629505134629506TG38GENIChomozygous138230355
7134630119134630120CA46GENIChomozygous138230356
7134630266134630267CT32GENIChomozygous138230357
7134630598134630599TC29GENIChomozygous138230358
7134631237134631238TG31GENIChomozygous138230359
7134631241134631242TC30GENIChomozygous138230360
7134631261134631262CG32GENIChomozygous138230361
7134631394134631395GT34GENICpossibly homozygous138230362
7134631521134631522GA63GENIChomozygous138230363
7134633169134633170AT46GENIChomozygous138230364
7134633602134633603AG43GENIChomozygous138230365
7134634272134634273GA43GENIChomozygous138230366
7134635216134635217AG38GENIChomozygous138230367
7134635302134635303GA39GENIChomozygous138230368
7134635865134635866GA41GENIChomozygous138230369
7134638039134638040TC15GENIChomozygous138230371
7134638457134638462TTTTG29GENIChomozygous137985587
7134638594134638595AG23GENIChomozygous138230372
7134639892134639893T37GENIChomozygous137985588
7134640388134640389GA44GENIChomozygous138230373
7134640855134640856GA35GENICpossibly homozygous138230374
7134642132134642133GT34GENIChomozygous138230375
7134642940134642940AG30GENIChomozygous137985590
7134643822134643823GA30GENICpossibly homozygous138230376
7134644325134644326GA59GENIChomozygous138230377
7134653114134653115CT40GENIChomozygous138230378
7134639892134639893TC37GENICheterozygous403228296