chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1180555765180555766TC20GENIChomozygous74620610
1180556517180556518AG36GENIChomozygous74620611
1180556553180556554GA38GENIChomozygous74620612
1180556692180556693AG50GENIChomozygous74620613
1180556888180556889AG42GENIChomozygous75721724
1180557024180557025CT33GENIChomozygous74620614
1180557490180557491AC29GENICpossibly homozygous74620615
1180557545180557546AT42GENIChomozygous74620616
1180557605180557606AT40GENIChomozygous75721726
1180557945180557946AC13GENICheterozygous76667263
1180558099180558100CT53GENICpossibly homozygous75721728
1180558222180558223GA40GENIChomozygous74620621
1180558749180558750GA27GENIChomozygous74620623
1180559463180559464CA36GENIChomozygous74620625
1180560024180560025CT43GENIChomozygous74620626
1180560534180560535AT45GENIChomozygous74620627
1180560551180560552TC43GENICpossibly homozygous76635864
1180560639180560640GA45GENIChomozygous74620628
1180560726180560727GA43GENIChomozygous75721730
1180560898180560899CT38GENIChomozygous75721732
1180562103180562104GA39GENIChomozygous75721734
1180562162180562163GC35GENIChomozygous75721736
1180562348180562349CG18GENICpossibly homozygous76378956
1180562611180562612AC32GENICpossibly homozygous75721738
1180563088180563089AG36GENIChomozygous74620631
1180563242180563243GT30GENIChomozygous75875458
1180563435180563436GA36GENIChomozygous74620633
1180563562180563563TG46GENIChomozygous74620634
1180563779180563780CT35GENIChomozygous74620635
1180563818180563819AG28GENIChomozygous74620636
1180563849180563850TC29GENIChomozygous74620637
1180563854180563855CT28GENIChomozygous75721740
1180564588180564589CT50GENIChomozygous75721742
1180566810180566811GC34GENIChomozygous74620641
1180570115180570116CG21GENICheterozygous76667264
1180571938180571939CT37GENIChomozygous75721744
1180572023180572024CT41GENIChomozygous75721746
1180579168180579169CT31GENIChomozygous74620696
1180588130180588131TC23GENIChomozygous74620741
1180588200180588201TC28GENIChomozygous74620742