chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1180555765180555766TC37GENICpossibly homozygous74620610
1180556517180556518AG45GENIChomozygous74620611
1180556553180556554GA46GENIChomozygous74620612
1180556692180556693AG30GENIChomozygous74620613
1180556888180556889AG23GENIChomozygous75721724
1180557024180557025CT18GENIChomozygous74620614
1180557490180557491AC31GENIChomozygous74620615
1180557545180557546AT34GENIChomozygous74620616
1180557605180557606AT28GENIChomozygous75721726
1180558099180558100CT17GENIChomozygous75721728
1180558222180558223GA25GENIChomozygous74620621
1180558749180558750GA45GENIChomozygous74620623
1180559463180559464CA28GENIChomozygous74620625
1180560024180560025CT49GENIChomozygous74620626
1180560534180560535AT5GENIChomozygous74620627
1180560550180560551TC3GENIChomozygous75788661
1180560639180560640GA19GENIChomozygous74620628
1180560726180560727GA27GENIChomozygous75721730
1180560898180560899CT26GENIChomozygous75721732
1180562103180562104GA37GENIChomozygous75721734
1180562162180562163GC42GENIChomozygous75721736
1180562611180562612AC26GENIChomozygous75721738
1180563088180563089AG60GENIChomozygous74620631
1180563435180563436GA14GENIChomozygous74620633
1180563562180563563TG22GENIChomozygous74620634
1180563779180563780CT31GENIChomozygous74620635
1180563818180563819AG34GENIChomozygous74620636
1180563849180563850TC37GENIChomozygous74620637
1180563854180563855CT39GENICpossibly homozygous75721740
1180564588180564589CT27GENIChomozygous75721742
1180566810180566811GC39GENIChomozygous74620641
1180571938180571939CT33GENIChomozygous75721744
1180572023180572024CT44GENIChomozygous75721746
1180579168180579169CT29GENIChomozygous74620696
1180588130180588131TC37GENIChomozygous74620741
1180588200180588201TC48GENIChomozygous74620742
1180563242180563243GT21GENIChomozygous75875458
1180587168180587169GT13GENIChomozygous75875459