chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106214111162141112AG26GENIChomozygous116613384
106214355162143552T9GENIChomozygous132692780
106214376162143772TTTTTTTTTTT2GENIChomozygous133758160
106214553462145535GA13GENIChomozygous116613390
106214782862147829AG22GENIChomozygous116613394
106214844362148444TC26GENIChomozygous116613396
106214995362149954AT21GENIChomozygous116790933
106215156562151566TC16GENIChomozygous116790935
106215841962158420CT20GENIChomozygous116613420
106216308362163084TC22GENIChomozygous116613426
106216483662164837TA29GENIChomozygous116790939
106214466762144668TA22GENIChomozygous116939603
106214730262147303GA23GENIChomozygous116939605
106215029862150299CT26GENIChomozygous116939607
106214605162146051GGGTCCCA20GENIChomozygous128822678
106215452162154522G15GENIChomozygous128822679
106215453962154540C23GENIChomozygous128822680
106215455762154558C24GENIChomozygous128822681
106215781862157818T26GENIChomozygous128822682
106216398062163981CA7GENIChomozygous116978454
106217660662176607CA31GENIChomozygous116790941
106217986162179862CT22GENIChomozygous116790943
106218012262180123TC18GENIChomozygous116613450
106218572262185723AG20GENIChomozygous117997323
106218617162186172TC30GENIChomozygous117104188
106218622962186230TC20GENIChomozygous117997326
106218933062189331TA24GENIChomozygous116613486
106217098062170981GA8GENIChomozygous118041086