chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1180555765180555766TC30GENICpossibly homozygous74620610
1180556517180556518AG21GENIChomozygous74620611
1180556553180556554GA24GENICpossibly homozygous74620612
1180556692180556693AG17GENICpossibly homozygous74620613
1180556888180556889AG25GENIChomozygous75721724
1180557024180557025CT31GENIChomozygous74620614
1180557490180557491AC19GENICpossibly homozygous74620615
1180557545180557546AT14GENICpossibly homozygous74620616
1180557605180557606AT27GENIChomozygous75721726
1180558222180558223GA21GENICpossibly homozygous74620621
1180558749180558750GA20GENICpossibly homozygous74620623
1180559463180559464CA22GENIChomozygous74620625
1180560024180560025CT34GENIChomozygous74620626
1180560534180560535AT17GENICpossibly homozygous74620627
1180560550180560551TC14GENIChomozygous75788661
1180560551180560552TC13GENIChomozygous76635864
1180560639180560640GA24GENIChomozygous74620628
1180560726180560727GA27GENIChomozygous75721730
1180560898180560899CT29GENICpossibly homozygous75721732
1180562103180562104GA23GENIChomozygous75721734
1180562162180562163GC24GENICpossibly homozygous75721736
1180562348180562349CG9GENIChomozygous76378956
1180562353180562354TC5GENIChomozygous76635865
1180562355180562356CT4GENIChomozygous76635866
1180562611180562612AC31GENICpossibly homozygous75721738
1180563088180563089AG22GENIChomozygous74620631
1180563435180563436GA16GENICpossibly homozygous74620633
1180563562180563563TG17GENICpossibly homozygous74620634
1180563779180563780CT24GENIChomozygous74620635
1180563818180563819AG21GENIChomozygous74620636
1180563849180563850TC32GENIChomozygous74620637
1180563854180563855CT30GENIChomozygous75721740
1180564588180564589CT32GENICpossibly homozygous75721742
1180566810180566811GC31GENIChomozygous74620641
1180571938180571939CT24GENIChomozygous75721744
1180572023180572024CT23GENIChomozygous75721746
1180579168180579169CT22GENIChomozygous74620696
1180588130180588131TC29GENIChomozygous74620741
1180588200180588201TC30GENICpossibly homozygous74620742