chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2195649884195649885AG33GENIChomozygous774422606
2195650907195650908AG36GENIChomozygous774422607
2195651871195651872AC41GENIChomozygous774422608
2195652699195652700TC52GENIChomozygous774422609
2195655859195655860CT30GENIChomozygous774422610
2195655866195655867AG27GENIChomozygous774422611
2195658665195658666AT26GENIChomozygous774422612
2195660620195660621AG61GENIChomozygous774422613
2195661310195661311AG16GENIChomozygous774422614
2195661700195661701CA51GENIChomozygous774422615
2195661951195661952GT37GENIChomozygous774422616
2195662348195662349TC37GENIChomozygous774422617
2195662753195662754TC52GENIChomozygous774422618
2195663363195663364GA43GENIChomozygous774422619
2195663500195663501CG59GENIChomozygous774422620
2195663525195663526AG56GENIChomozygous774422621
2195663528195663529AG57GENIChomozygous774422622
2195664478195664479AG33GENICpossibly homozygous774422623
2195664536195664537GA38GENICheterozygous774422624
2195664662195664663CA26GENIChomozygous774422625
2195665229195665230CT33GENIChomozygous774422626
2195665357195665358TC48GENIChomozygous774422627
2195665990195665991TC14GENIChomozygous774422628
2195666506195666507CT26GENIChomozygous774422629
2195667404195667405TC40GENICpossibly homozygous774422630
2195667847195667848AT29GENIChomozygous774422631