chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4152892649152892650AG4GENIChomozygous112888862
4152897351152897352GA14GENIChomozygous112888863
4152897380152897381TG18GENIChomozygous112888864
4152897382152897383CT17GENIChomozygous112888865
4152897452152897453CT16GENIChomozygous112888866
4152900198152900199CT9GENIChomozygous112888868
4152900560152900561GA9GENIChomozygous112888869
4152903431152903432CT16GENIChomozygous112888870
4152903894152903895GT22GENIChomozygous112888871
4152905997152905998AG4GENIChomozygous112888872
4152909728152909729GC23GENIChomozygous112888875
4152910422152910423TC6GENIChomozygous112888883
4152910843152910844CA21GENIChomozygous112888884
4152914584152914585CT10GENIChomozygous112888885
4152918774152918775GA31GENIChomozygous112888886
4152922228152922229AG17GENIChomozygous112888887
4152922714152922715AC16GENIChomozygous112888888
4152924679152924680TC9GENIChomozygous112888889
4152925732152925733TG5GENIChomozygous112888890
4152925739152925740CT8GENIChomozygous112888891
4152930457152930458CT25GENIChomozygous112888893
4152932289152932290GA22GENIChomozygous112888894
4152933044152933045CA4GENIChomozygous112888895
4152936748152936749GA17GENIChomozygous112888897
4152937021152937022CT8GENIChomozygous112888898
4152937409152937410AC14GENIChomozygous112888899
4152937458152937459GA7GENIChomozygous112888900
4152938627152938628TC12GENICheterozygous112888903
4152943095152943096AG12GENIChomozygous112888904
4152947830152947831GT11GENIChomozygous112888905
4152950586152950587TC7GENIChomozygous112888906
4152954960152954961TC19GENIChomozygous112888911
4152956926152956927TC11GENIChomozygous112888912
4152957095152957096CG5GENIChomozygous112888913
4152959064152959065GT27GENIChomozygous112888914
4152960112152960113AG13GENIChomozygous112888915
4152962014152962015CT12GENIChomozygous112888916
4152962418152962419GA18GENIChomozygous112888917
4152970206152970207AG11GENIChomozygous112888919
4152971313152971314GT38GENIChomozygous112888920