chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191049554810495549TC31GENIChomozygous109634042
191049571710495718TC20GENIChomozygous110169046
191049573810495739TC18GENIChomozygous110169048
191049575110495752GA10GENIChomozygous110169050
191049630010496301GT44GENIChomozygous109634048
191049690510496906GC30GENIChomozygous109634050
191049838710498388CT31GENIChomozygous109634052
191049967910499680GA38GENIChomozygous109634054
191050038610500387GT24GENIChomozygous109634056
191050575110505752GA34GENICpossibly homozygous109634058
191049572710495728GT22GENICpossibly homozygous110058358
191049576310495764CA8GENIChomozygous119596328
191049869510498696CG26GENICpossibly homozygous119722035
191050500110505002TC121GENICheterozygous110098979
191051407610514077CG5GENIChomozygous109634060
191051407810514079AG5GENIChomozygous109634062
191051454210514543CT41GENIChomozygous109634064
191051459310514594AG39GENIChomozygous109634066
191051463610514637GA45GENIChomozygous109634068
191051402810514029GA8GENIChomozygous109799513