chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124394295124394296CT21GENIChomozygous126539516
7124394937124394938GA12GENIChomozygous126539517
7124397388124397389GA15GENIChomozygous126539518
7124397831124397832GA15GENIChomozygous126539519
7124399198124399199AC9GENIChomozygous126539520
7124399484124399485AG23GENIChomozygous126539521
7124399728124399729CT21GENIChomozygous126539522
7124400618124400619CT19GENIChomozygous126539523
7124400937124400938AC14GENIChomozygous126539524
7124400948124400949AG13GENIChomozygous126539525
7124401278124401279AC8GENIChomozygous126539526
7124401288124401289GA7GENIChomozygous126539527
7124401615124401616CA20GENIChomozygous126539528
7124401818124401819AC18GENIChomozygous126539529
7124401999124402000CT19GENIChomozygous126539530
7124402424124402425TC21GENIChomozygous126539531
7124405702124405703GA22GENIChomozygous126539532
7124405733124405734GA24GENIChomozygous126539533
7124408153124408154TC10GENIChomozygous126539534
7124408713124408714TC6GENIChomozygous126539535
7124409395124409396AG24GENIChomozygous126539536
7124409643124409644GT14GENIChomozygous126539537