chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172204859222048593AG26GENIChomozygous110990719
172204863622048637TC18GENIChomozygous110990721
172204870822048709AG13GENIChomozygous110990723
172204877322048774CG24GENIChomozygous110990725
172204879022048791TC24GENIChomozygous110990727
172204879122048792GA24GENIChomozygous110990729
172204885522048856AC30GENIChomozygous110990731
172204888222048883TC28GENIChomozygous110990733
172204895422048955AG26GENIChomozygous110990735
172204905822049059CT30GENIChomozygous110990737
172204908922049090GA33GENIChomozygous110990741
172204915622049157CA41GENIChomozygous110990743
172204931222049313CG44GENIChomozygous110990747
172204932322049324TA45GENIChomozygous110990749
172204943322049434TG36GENIChomozygous110990751
172204946122049462GA31GENIChomozygous111413696
172204953622049537AG30GENIChomozygous110990753
172204954622049547CT33GENIChomozygous110990755
172204986322049864TG23GENIChomozygous111234590
172205131222051313GA17GENIChomozygous110990759
172205160622051607TC30GENIChomozygous110990761
172205176722051768GA29GENIChomozygous110990763
172205354822053549GT31GENICheterozygous111413698
172205374322053744TC25GENIChomozygous110990771
172205434122054342AG19GENIChomozygous110990773
172205515622055157GA20GENIChomozygous111234596
172205524822055249TC17GENIChomozygous111413700
172205580022055801TC26GENIChomozygous111234598
172205593822055939CA26GENIChomozygous111413702
172205641122056412TA35GENIChomozygous111234606
172205706622057067AC41GENIChomozygous111413704
172205742022057421GA25GENIChomozygous110990779
172205778022057781TG6GENIChomozygous111178688
172206066922060670GT18GENIChomozygous111413706
172206756122067562GA33GENIChomozygous110990801
172205804222058043AG13GENICheterozygous119270160
172205804722058048CG13GENICheterozygous119270161
172206375722063758TC10GENIChomozygous119270162
172206035922060360TC18GENIChomozygous111445861
172206375522063756TG10GENIChomozygous111496900