chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105901370659013707CT18GENIChomozygous116937388
105901463159014632AC29GENIChomozygous116937390
105901498959014990TC19GENIChomozygous116607644
105901535659015357CT23GENIChomozygous116937392
105901717059017171TC10GENIChomozygous116937394
105901766059017661CT23GENIChomozygous116937396
105901834359018344TC26GENIChomozygous116937398
105901869859018699GA14GENIChomozygous116937400
105902121159021212TC13GENIChomozygous116788218
105902124259021243GA13GENIChomozygous116937402
105902232359022324AG20GENIChomozygous116607646
105902321459023215GA20GENIChomozygous116937404
105902760959027610AG28GENIChomozygous116788228
105903172759031728CT6GENIChomozygous116937406
105903864359038644CT18GENIChomozygous116788232
105904129859041299CG15GENIChomozygous116937408
105904130959041310CA15GENIChomozygous116937410
105904625359046254GA21GENIChomozygous116937412