chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150005982150005983TC55GENIChomozygous114054593
5150006619150006620TG34GENIChomozygous114054595
5150006650150006651GA44GENIChomozygous114054597
5150008225150008226TC50GENIChomozygous114054603
5150008806150008807TC50GENIChomozygous114054605
5150008824150008825GA53GENIChomozygous114054607
5150009005150009006GC33GENIChomozygous114054609
5150009007150009008TA34GENIChomozygous114054611
5150012011150012012TC35GENIChomozygous114054613
5150012096150012097AG43GENIChomozygous114054615
5150013500150013501GA57GENIChomozygous114054617
5150014830150014831AG55GENIChomozygous114054619
5150015545150015546TC54GENIChomozygous114054621
5150018207150018208AG47GENIChomozygous114054623
5150018714150018715AG30GENIChomozygous114054625
5150019188150019189TG46GENIChomozygous114054627
5150020477150020478GA52GENIChomozygous114054629
5150021617150021618TC61GENIChomozygous114054631
5150022689150022690CA41GENIChomozygous114054633
5150022690150022691CT41GENIChomozygous114054635
5150023006150023007GC40GENIChomozygous114054637
5150023959150023960GA52GENIChomozygous114054639
5150026630150026631CT48GENIChomozygous114054641
5150026754150026755TA46GENIChomozygous114054643
5150026866150026867CT52GENIChomozygous114054645
5150027118150027119AG49GENIChomozygous114054647