chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7107695637107695638AG14GENIChomozygous115807964
7107697562107697563CT23GENIChomozygous115807966
7107698638107698639GT17GENIChomozygous115807968
7107698694107698695GA12GENIChomozygous115807970
7107699044107699045CA18GENIChomozygous115807972
7107699920107699921TC19GENIChomozygous115807976
7107700548107700549AG16GENIChomozygous115807978
7107702382107702383AG10GENIChomozygous115807982
7107703373107703374GT17GENIChomozygous115807984
7107703556107703557CT17GENIChomozygous115807986
7107703575107703576CT21GENIChomozygous115807988
7107703606107703607GA18GENIChomozygous115807990
7107703909107703910CT18GENIChomozygous115807992
7107705110107705111GA27GENIChomozygous115807994
7107707537107707538GA25GENIChomozygous115807996
7107708029107708030TC19GENIChomozygous115807998
7107709747107709748AG23GENIChomozygous115808000
7107711540107711541AG23GENIChomozygous115808002
7107712278107712279CT33GENIChomozygous115808004
7107714923107714924GA27GENIChomozygous115808010
7107717668107717669GT17GENIChomozygous115808012
7107720537107720538CG26GENIChomozygous115808016
7107721577107721578GA27GENIChomozygous115808018
7107721736107721737GA30GENIChomozygous115808020
7107722906107722907AG15GENIChomozygous115808022
7107722931107722932AG13GENIChomozygous115808024