chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167032773170327732AG41GENICpossibly homozygous47690906
167032808570328086TC43GENICpossibly homozygous47690907
167032820970328210AC31GENIChomozygous47863868
167032855770328558GC45GENIChomozygous47690909
167032857370328574TA47GENIChomozygous47863870
167032859470328595TA48GENIChomozygous47863872
167032874670328747TA45GENIChomozygous47863874
167032894370328944AG40GENIChomozygous47863876
167032979970329800GA17GENICheterozygous47690910
167032982070329821G-17GENIChomozygous47863878
167033017170330172TC50GENIChomozygous47690911
167033019370330194CT54GENIChomozygous47863880
167033045070330451T-31GENIChomozygous47863882
167033067070330671TC55GENICpossibly homozygous47863884
167033086470330865CT52GENIChomozygous47863886
167033147770331478TA15GENIChomozygous47690913
167033194670331947TC36GENIChomozygous47863888