chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106363807563638076TC13GENIChomozygous51902867
106363819863638199TA26GENIChomozygous51902869
106363849363638494GA24GENIChomozygous51902871
106363859163638592AG18GENIChomozygous51902873
106363881563638816CG26GENIChomozygous51902875
106363891863638919GGAA22GENICheterozygous51672480
106363891863638919GGA22GENICheterozygous51902877
106363891963638920A-22GENICheterozygous52062898
106364034163640342AG24GENIChomozygous51902879
106364100263641003CG19GENIChomozygous51902881
106364187563641876AG13GENIChomozygous51902883
106364207063642071AG29GENIChomozygous51902885
106364655463646555AG24GENIChomozygous51475153
106364657863646579TC24GENIChomozygous51902887
106364659763646598CA25GENIChomozygous51475154
106364665763646658CT16GENIChomozygous51902890
106364711063647111GA25GENIChomozygous51902892
106364724463647245AG25GENIChomozygous51902894
106364756963647570G-23GENIChomozygous51902896
106364768763647697ACAAAACAAA----------9GENIChomozygous51902898