chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
204308497843084979TC18GENIChomozygous125207126
204308761043087611AG19GENIChomozygous125207127
204308870443088705TC5GENICheterozygous125207128
204308893043088931TC11GENIChomozygous125207129
204309076743090768TC4GENICheterozygous125197002
204309086043090861CA9GENIChomozygous125194839
204309052443090525TC9GENIChomozygous125214628
204309068643090687CA7GENIChomozygous125214629
204309069743090698CA6GENIChomozygous125214630
204309062743090628TC12GENIChomozygous125194836
204309064943090650TC11GENIChomozygous125194837
204309084043090841TC5GENIChomozygous125194838
204309070143090702CA7GENIChomozygous125219638
204309088443090885TC14GENIChomozygous125194840
204309089843090899TC16GENIChomozygous125194841
204309127943091280CT23GENIChomozygous125207132
204309260943092610AC11GENIChomozygous125207133
204309320543093206CT15GENIChomozygous125207134
204309352143093522TC16GENIChomozygous125207135
204309651643096517TC7GENIChomozygous125207136
204309714143097142AG25GENIChomozygous125207137
204309834143098342GA9GENIChomozygous125214632
204309849343098494AC29GENIChomozygous125207138
204309888543098886TA17GENIChomozygous125207139
204309940743099408GA13GENIChomozygous125207140
204309957743099578CT21GENIChomozygous125207141
204309965643099657TC19GENIChomozygous125207142
204310042043100421GA20GENIChomozygous125207143
204310136143101362CT18GENIChomozygous125207144
204310232243102323TA5GENIChomozygous125214633
204310734743107348GA22GENIChomozygous125207150
204310263443102635TC24GENIChomozygous125207145
204310291943102920TG13GENIChomozygous125207146
204310439843104399CT17GENIChomozygous125207147
204310470243104703AG17GENIChomozygous125207148
204310694743106948GA16GENIChomozygous125207149