chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122201413722014138CCA14GENIChomozygous50537938
122201433822014343ATTAT-----9GENICheterozygous50597401
122201593122015934ACC---18GENICheterozygous50557534
122201746622017467T-7GENICheterozygous50537941
122201831722018318T-2GENIChomozygous50113755
122201854122018551CTCATAACAC----------29GENIChomozygous50597403
122201855322018557TGAC----28GENIChomozygous50597405
122201879822018800CG--1GENIChomozygous50561350
122201881122018812TTTA4GENICheterozygous50561352
122201886222018864GC--3GENICheterozygous50537942
122202254022022541GGA1GENIChomozygous50600502
122202257122022572GGA1GENIChomozygous50600503
122202257322022574GGGGGAA1GENIChomozygous50600504
122202262722022628GGA2GENIChomozygous50600505
122202266822022670AG--9GENIChomozygous50537945
122202275022022751TTA6GENIChomozygous50113794
122202279222022793AAC13GENIChomozygous50113800
122202285422022855AG18GENIChomozygous50113806
122202288422022885TC12GENIChomozygous50113808
122202288622022887GT12GENIChomozygous50113810
122202291222022913GC17GENIChomozygous50113812
122202298622022987CG16GENIChomozygous50113814
122202303222023033TG9GENIChomozygous50113816
122202305222023053AG9GENIChomozygous50113818
122202307022023071AG12GENIChomozygous50113820
122202307422023075AC13GENIChomozygous50113822
122202308022023081AG16GENIChomozygous50113824
122202313922023140GA21GENIChomozygous50113826
122202316222023163GA19GENIChomozygous50113828
122202316822023169GGAAC18GENIChomozygous50113830
122202319822023199CA11GENIChomozygous50113832
122202322222023223GA7GENIChomozygous50113834
122202323622023237AG5GENIChomozygous50113836