chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----29GENIChomozygous685485009
3154514276154514277TG43GENICpossibly homozygous506797997
3154514414154514415AAGTCT30GENIChomozygous685485010
3154514475154514476TC50GENIChomozygous506797998
3154514477154514478TC51GENICpossibly homozygous506797999
3154515475154515476GA23GENIChomozygous506798000
3154515681154515682TA59GENIChomozygous506798001
3154516008154516009GA51GENIChomozygous506798002
3154516260154516261TC53GENIChomozygous506798003
3154516884154516885AG56GENIChomozygous506798004
3154517077154517078TC64GENIChomozygous509353643
3154517156154517157AG63GENIChomozygous506798005
3154517593154517594TC62GENICpossibly homozygous506798006
3154517632154517633G-47GENIChomozygous685485011
3154517898154517899TC50GENIChomozygous506798007
3154517982154517986GGCA----52GENIChomozygous685485012
3154518068154518069GA60GENIChomozygous506798008
3154518158154518159TTA50GENIChomozygous685485013
3154518562154518563CT43GENIChomozygous509353644
3154518737154518738AG55GENIChomozygous506798009
3154518931154518932GGT25GENIChomozygous685485014
3154519100154519101CT43GENIChomozygous509353645
3154519184154519185CCA38GENIChomozygous685485015
3154519315154519316CT49GENICpossibly homozygous506798010
3154519630154519636TCCCTC------37GENICheterozygous685485017
3154519645154519646CG47GENICpossibly homozygous506798011
3154519651154519652GC44GENIChomozygous506798012
3154519896154519897CCTT18GENIChomozygous685485019
3154519985154519986AG69GENIChomozygous506798013
3154520058154520059TC61GENIChomozygous506798014
3154520781154520782TC54GENIChomozygous506798015
3154520987154520988CT55GENIChomozygous506798016
3154521914154521915TTAA22GENIChomozygous685485020
3154521930154521931AAC37GENICheterozygous685485021
3154522134154522135AG78GENICpossibly homozygous506798017