chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212727237212727241TTTG----19GENICheterozygous61076601
1212729890212729891AG13GENICheterozygous61076604
1212731180212731181CCAGAT11GENICheterozygous61076605
1212731849212731850AG19GENICheterozygous61076606
1212732133212732134TA16GENICheterozygous61076607
1212732283212732284TC18GENICheterozygous61076608
1212732898212732899AG21GENICheterozygous61076609
1212732908212732909GA23GENICheterozygous61076610
1212733279212733280AG13GENICheterozygous61076611
1212733415212733416TC10GENICheterozygous61076612
1212734086212734087CG10GENICheterozygous61076617
1212734571212734572CT18GENICheterozygous61076618
1212734635212734636TC28GENICheterozygous61076619
1212736629212736630CT17GENICheterozygous61076624
1212735014212735015TTC16GENICheterozygous61076620
1212735154212735155AG14GENICheterozygous61076621
1212736346212736376GCTGTGTCCCTTGTGTAGACAGGCATGCTG------------------------------22GENICheterozygous62098804
1212736674212736675AT22GENICheterozygous61076625
1212736689212736690GA22GENICheterozygous61076626
1212737698212737699TC17GENICheterozygous61076627
1212738397212738398TG22GENICheterozygous61076628
1212738749212738750GA24GENICheterozygous61076629
1212738832212738833AG23GENICheterozygous62484884