chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212727237212727241TTTG----16GENIChomozygous61076601
1212728962212728963GGA22GENIChomozygous61076602
1212729493212729494CCT2GENICheterozygous61076603
1212729890212729891AG16GENIChomozygous61076604
1212731180212731181CCAGAT15GENIChomozygous61076605
1212731849212731850AG34GENICpossibly homozygous61076606
1212732133212732134TA33GENIChomozygous61076607
1212732283212732284TC21GENIChomozygous61076608
1212732898212732899AG26GENIChomozygous61076609
1212732908212732909GA27GENIChomozygous61076610
1212733279212733280AG19GENIChomozygous61076611
1212733415212733416TC19GENIChomozygous61076612
1212733737212733738CCA6GENICheterozygous61076613
1212733767212733768A-7GENIChomozygous61076614
1212733790212733791CA11GENIChomozygous61076615
1212733798212733799AAC10GENICheterozygous62098803
1212734086212734087CG17GENIChomozygous61076617
1212734571212734572CT12GENIChomozygous61076618
1212734635212734636TC19GENIChomozygous61076619
1212735014212735015TTC31GENIChomozygous61076620
1212735154212735155AG10GENIChomozygous61076621
1212736346212736376GCTGTGTCCCTTGTGTAGACAGGCATGCTG------------------------------16GENIChomozygous62098804
1212736629212736630CT24GENIChomozygous61076624
1212736674212736675AT19GENIChomozygous61076625
1212736689212736690GA17GENIChomozygous61076626
1212736764212736765GGTGTGTCTGTGTC6GENIChomozygous62196080
1212737698212737699TC12GENIChomozygous61076627
1212738397212738398TG23GENIChomozygous61076628
1212738749212738750GA18GENIChomozygous61076629