chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7107695637107695638AG18GENIChomozygous115807964
7107697562107697563CT21GENIChomozygous115807966
7107698638107698639GT20GENIChomozygous115807968
7107698694107698695GA17GENIChomozygous115807970
7107699044107699045CA9GENIChomozygous115807972
7107699174107699175GA17GENIChomozygous115807974
7107699920107699921TC19GENIChomozygous115807976
7107701417107701418AC15GENICheterozygous115807980
7107702382107702383AG27GENIChomozygous115807982
7107703373107703374GT19GENIChomozygous115807984
7107703556107703557CT13GENIChomozygous115807986
7107703575107703576CT11GENIChomozygous115807988
7107703606107703607GA10GENIChomozygous115807990
7107703909107703910CT10GENIChomozygous115807992
7107705110107705111GA23GENIChomozygous115807994
7107706608107706609TA4GENICheterozygous118416613
7107707537107707538GA11GENIChomozygous115807996
7107708029107708030TC23GENIChomozygous115807998
7107709747107709748AG24GENIChomozygous115808000
7107710021107710022AC14GENICheterozygous118284720
7107711540107711541AG13GENIChomozygous115808002
7107712278107712279CT18GENIChomozygous115808004
7107714398107714399GC6GENIChomozygous122836498
7107714819107714820CT17GENIChomozygous115808006
7107714872107714873CT24GENIChomozygous115808008
7107714923107714924GA18GENIChomozygous115808010
7107717668107717669GT10GENIChomozygous115808012
7107719050107719051CT23GENICpossibly homozygous115808014
7107720537107720538CG23GENIChomozygous115808016
7107721577107721578GA27GENIChomozygous115808018
7107721736107721737GA19GENIChomozygous115808020
7107722906107722907AG20GENICpossibly homozygous115808022
7107722931107722932AG13GENIChomozygous115808024