chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171226171512261716AT1GENIChomozygous125624182
171226254112262541C4GENIChomozygous129423637
171226256712262568T6GENIChomozygous129423638
171226259712262598AC11GENIChomozygous111295162
171226263912262639A6GENIChomozygous129423639
171226264212262642CT6GENIChomozygous129423640
171226264912262649C6GENIChomozygous129423641
171226268612262686T5GENIChomozygous129423642
171226271412262714C5GENIChomozygous129423643
171226324212263243CG9GENIChomozygous111295163
171226324412263244G10GENIChomozygous129423654
171226325312263254AC10GENIChomozygous111295164
171226325612263257C10GENIChomozygous129423655
171226326112263269AAGGTATC10GENIChomozygous129423656
171226327912263281CT12GENIChomozygous129423657
171226259812262599CA11GENIChomozygous111315144
171226273212262732C4GENIChomozygous130165015
171226273312262734GA4GENIChomozygous130168617
171226401112264011T12GENIChomozygous131751071
171226754212267542G10GENIChomozygous131751072
171226536112265362CG21GENIChomozygous111669521
171226726512267266TC21GENIChomozygous110959547
171226619612266197AG27GENIChomozygous111333228
171226875512268756AG28GENIChomozygous111333230
171227018812270189AG18GENIChomozygous110959549
171227057912270579A23GENICpossibly homozygous131751073
171227176212271763AG18GENIChomozygous111333232
171227185112271851GTCTCA24GENIChomozygous131751074
171227186012271861AG22GENIChomozygous111333233
171227309612273097CT24GENIChomozygous111333235
171227362512273626T23GENIChomozygous131751075
171227394912273950TC21GENIChomozygous111333237
171227406012274060A9GENIChomozygous131751076
171227331412273315CT24GENIChomozygous111525756
171227066512270666CA23GENIChomozygous111525754