chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
112418172624181727GA21GENIChomozygous991644614
112418279024182791GA17GENIChomozygous991644615
112418400424184005GT20GENIChomozygous991644616
112418400724184008TG22GENIChomozygous991644617
112418445924184460CA14GENIChomozygous991644618
112418490724184908AG12GENIChomozygous991644619
112418531824185319CA28GENIChomozygous991644620
112418567024185671TC32GENIChomozygous991644621
112418668324186684AT18GENIChomozygous991644622
112418684124186842GA18GENIChomozygous991644623
112418693024186931CT17GENIChomozygous991644624
112418718524187186AC12GENIChomozygous991644625
112418761624187617CT26GENIChomozygous991644626
112418796924187970CT25GENIChomozygous991644627
112418816124188162GA20GENIChomozygous991644628
112418862824188629AC29GENIChomozygous991644629
112418968824189689TC22GENIChomozygous991644630
112419055224190553CT27GENIChomozygous991644631
112419055524190556GA28GENIChomozygous991644632
112419071024190711AT13GENIChomozygous991644633
112419204924192050AG6GENIChomozygous991644634
112419206224192063CG6GENIChomozygous991644635
112419209324192094GT2GENIChomozygous991644636
112419210324192104CG2GENIChomozygous991644637
112419210424192105GC2GENIChomozygous991644638
112419265424192655CT23GENIChomozygous991644639
112419282224192823CT23GENIChomozygous991644640