chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1180555765180555766TC14GENIChomozygous74620610
1180556517180556518AG33GENIChomozygous74620611
1180556553180556554GA37GENIChomozygous74620612
1180556692180556693AG38GENIChomozygous74620613
1180556888180556889AG28GENIChomozygous75721724
1180557024180557025CT23GENIChomozygous74620614
1180557490180557491AC29GENIChomozygous74620615
1180557545180557546AT24GENIChomozygous74620616
1180557605180557606AT31GENIChomozygous75721726
1180558099180558100CT3GENIChomozygous75721728
1180558222180558223GA16GENIChomozygous74620621
1180558749180558750GA16GENIChomozygous74620623
1180559463180559464CA29GENIChomozygous74620625
1180560024180560025CT32GENIChomozygous74620626
1180560534180560535AT17GENIChomozygous74620627
1180560551180560552TC19GENIChomozygous76635864
1180560639180560640GA22GENIChomozygous74620628
1180560726180560727GA25GENIChomozygous75721730
1180560898180560899CT48GENICpossibly homozygous75721732
1180562103180562104GA32GENICpossibly homozygous75721734
1180562162180562163GC28GENIChomozygous75721736
1180562611180562612AC32GENIChomozygous75721738
1180563088180563089AG29GENIChomozygous74620631
1180563435180563436GA32GENIChomozygous74620633
1180563562180563563TG34GENIChomozygous74620634
1180563779180563780CT38GENIChomozygous74620635
1180563818180563819AG27GENIChomozygous74620636
1180563849180563850TC32GENIChomozygous74620637
1180563854180563855CT32GENIChomozygous75721740
1180564588180564589CT30GENIChomozygous75721742
1180566810180566811GC34GENIChomozygous74620641
1180571938180571939CT37GENIChomozygous75721744
1180572023180572024CT45GENIChomozygous75721746
1180579168180579169CT28GENIChomozygous74620696
1180588130180588131TC34GENIChomozygous74620741
1180588200180588201TC32GENIChomozygous74620742