chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144367059943670600A-21GENIChomozygous764129605
144367192543671926AG22GENICpossibly homozygous661739524
144367218343672184TTATAAA33GENIChomozygous764129606
144367233743672338TC29GENIChomozygous661739525
144367277143672772GA28GENIChomozygous661739526
144367295643672957AG33GENIChomozygous661739527
144367343743673438AT37GENIChomozygous661739528
144367381643673817CT14GENIChomozygous661739529
144367394343673945TT--19GENIChomozygous764129607
144367398943673990CCCTTG21GENIChomozygous764129609
144367436243674363GA27GENIChomozygous661739530
144367437543674376TC24GENIChomozygous661739531
144367454943674550CG14GENIChomozygous661739532
144367495043674951GT14GENIChomozygous661739533
144367506243675063AACCC6GENIChomozygous764129612
144367511343675116AAA---15GENIChomozygous764129613
144367511943675120AG17GENIChomozygous661739534
144367525343675254CT19GENIChomozygous661739535
144367566243675663AG22GENIChomozygous661739536
144367662343676624AG26GENIChomozygous661739537