chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
136054781260547813AC18GENIChomozygous114625045
136054819060548191TG28GENIChomozygous114365638
136054825160548252TC18GENIChomozygous114365639
136054872360548724CT26GENIChomozygous114625049
136054882560548826GT36GENIChomozygous114625051
136054942160549422CT18GENIChomozygous114625053
136054949160549492GA13GENIChomozygous114625055
136054979660549797CT20GENIChomozygous114625057
136054989760549898AG30GENIChomozygous114625059
136054990960549910AG26GENIChomozygous114365641
136055014360550144TA36GENIChomozygous114365643
136055030460550305TC30GENIChomozygous114365644
136055078160550782CA25GENIChomozygous114625063
136055218160552182TC25GENIChomozygous114365646
136055237460552375GT23GENIChomozygous114625065
136055271060552711TA31GENIChomozygous114625067
136055271260552713TA32GENIChomozygous114625069
136055377360553774TC29GENIChomozygous114365648
136055411160554112CT26GENIChomozygous114625071
136055438160554382AT16GENIChomozygous114625073
136055488360554884TG24GENIChomozygous114365651
136055490760554908TC21GENIChomozygous114365652
136055552860555529CG19GENIChomozygous114365655
136055590060555901TG10GENIChomozygous114365656
136055590160555902CT10GENIChomozygous114625075
136055753060557531AC18GENIChomozygous114625077
136055798960557990GA27GENIChomozygous114558271
136056218260562183GC19GENIChomozygous114365662
136056223060562231CT18GENIChomozygous114365663
136056239660562397AG25GENIChomozygous114365665
136056320160563202AG18GENIChomozygous114625079
136056322460563225TC19GENIChomozygous114365666
136056344160563442TA19GENIChomozygous114365667
136056412160564122AC25GENIChomozygous114625081
136056413660564137CT25GENIChomozygous114365668
136056427560564276CT24GENIChomozygous114365669
136056427660564277TA24GENIChomozygous114365670
136056516060565161CA24GENIChomozygous114625083
136056548660565487GA31GENIChomozygous114365671
136056572960565730GA27GENIChomozygous114625085
136056614760566148AT10GENIChomozygous114625087