chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124247956142479562AT34GENIChomozygous50209153
124247956642479567TG35GENIChomozygous50209154
124247957242479573TC36GENIChomozygous50209155
124248066042480661CCCA13GENICheterozygous50209156
124248395342483954T-26GENICheterozygous50209159
124248397142483972C-44GENICheterozygous50209160
124248583142485832AG26GENIChomozygous50209163
124248612842486129AG26INTERGENIChomozygous50209164
124248627042486271AAC16INTERGENICpossibly homozygous50209165
124248627842486279AC18INTERGENIChomozygous50209166
124248629342486296GTG---14INTERGENICheterozygous50327509
124248630842486309AT15INTERGENICpossibly homozygous50327511
124248719442487195GA66GENIChomozygous50327513
124248770642487707CT46GENIChomozygous50209168
124248811342488114AATTT10GENICpossibly homozygous50209170
124248840642488407TTTC36GENICpossibly homozygous50209171
124248841142488421TTTTTTTTAA----------29GENIChomozygous50209172
124248841242488421TTTTTTTAA---------29GENICheterozygous50209173
124248845542488456C-28GENIChomozygous50327515
124249059342490594AG28GENICpossibly homozygous50327517
124249059542490596A-28GENIChomozygous50327519
124249060342490609CACACA------20GENIChomozygous50327521
124249060742490608CCG27GENICheterozygous50327523
124249065742490658CT49GENIChomozygous50209180
124249123642491237A-38GENIChomozygous50327525
124249291842492919CT49GENIChomozygous50327527
124249410142494102CA74INTERGENIChomozygous50209183