chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55969008759690088GA17GENICheterozygous403142912
55969008759690088G17GENICheterozygous403142913
55969008859690089G17GENICheterozygous403718820
55969008859690089GA17GENICheterozygous403718821
55969117859691178CCCCCCAAA5GENICheterozygous147262218
55969123459691235G22GENICheterozygous403142918
55969123459691235GT22GENICheterozygous403142919
55971075759710758CG12GENICheterozygous404582635
55971075759710758C12GENICheterozygous404582636
55972407859724079AT24GENICheterozygous403142925
55972407859724079A24GENICheterozygous403142926
55972408059724081AT24GENICheterozygous403142927
55972408059724081A24GENICheterozygous403142928
55974992759749928GT10GENICheterozygous403142937
55969124759691248GA24GENIChomozygous137480191
55974992759749928G10GENICpossibly homozygous403142938
55974992859749929G10GENICpossibly homozygous404397177
55974992859749929GT10GENICheterozygous404397178