chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124394295124394296CT20GENIChomozygous126539516
7124394937124394938GA4GENIChomozygous126539517
7124397388124397389GA13GENIChomozygous126539518
7124397831124397832GA12GENIChomozygous126539519
7124399198124399199AC7GENIChomozygous126539520
7124399484124399485AG19GENICpossibly homozygous126539521
7124399728124399729CT20GENIChomozygous126539522
7124400618124400619CT15GENIChomozygous126539523
7124400937124400938AC12GENIChomozygous126539524
7124400948124400949AG11GENIChomozygous126539525
7124401278124401279AC8GENIChomozygous126539526
7124401288124401289GA9GENIChomozygous126539527
7124401615124401616CA6GENIChomozygous126539528
7124401818124401819AC25GENIChomozygous126539529
7124401999124402000CT25GENIChomozygous126539530
7124402424124402425TC14GENIChomozygous126539531
7124405702124405703GA35GENIChomozygous126539532
7124405733124405734GA24GENIChomozygous126539533
7124408153124408154TC15GENIChomozygous126539534
7124409395124409396AG20GENIChomozygous126539536
7124409643124409644GT12GENIChomozygous126539537
7124404703124404704CT5GENIChomozygous126602329