chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7107695637107695638AG25GENIChomozygous115807964
7107697562107697563CT29GENIChomozygous115807966
7107698638107698639GT27GENIChomozygous115807968
7107698694107698695GA28GENIChomozygous115807970
7107699044107699045CA19GENIChomozygous115807972
7107699174107699175GA17GENIChomozygous115807974
7107699920107699921TC26GENIChomozygous115807976
7107700548107700549AG19GENIChomozygous115807978
7107702382107702383AG25GENIChomozygous115807982
7107703373107703374GT17GENIChomozygous115807984
7107703556107703557CT19GENIChomozygous115807986
7107703575107703576CT16GENIChomozygous115807988
7107703606107703607GA10GENIChomozygous115807990
7107703909107703910CT17GENIChomozygous115807992
7107705110107705111GA32GENIChomozygous115807994
7107707537107707538GA24GENIChomozygous115807996
7107708029107708030TC21GENIChomozygous115807998
7107709747107709748AG24GENIChomozygous115808000
7107711540107711541AG20GENIChomozygous115808002
7107712278107712279CT28GENIChomozygous115808004
7107714819107714820CT26GENIChomozygous115808006
7107714872107714873CT24GENIChomozygous115808008
7107714923107714924GA27GENIChomozygous115808010
7107717668107717669GT25GENIChomozygous115808012
7107719050107719051CT26GENIChomozygous115808014
7107720537107720538CG29GENIChomozygous115808016
7107721577107721578GA34GENIChomozygous115808018
7107721736107721737GA23GENIChomozygous115808020
7107722906107722907AG25GENIChomozygous115808022
7107722931107722932AG24GENIChomozygous115808024