chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124247956142479562AT12GENIChomozygous50209153
124247956642479567TG11GENIChomozygous50209154
124247957242479573TC11GENIChomozygous50209155
124248066042480661CCCA5GENIChomozygous50209156
124248311442483157AGATGGGTGCTCTTAACCGCTGAGCCATCTCTCCAGCCCCCCC-------------------------------------------16GENICheterozygous50544349
124248395242483953GGT10GENICheterozygous50209158
124248395442483955T-10GENICheterozygous50563860
124248770642487707CT22GENIChomozygous50209168
124248811342488114AATTTTT7GENICheterozygous50544352
124248841142488421TTTTTTTTAA----------14GENICpossibly homozygous50209172
124248502842485029GGT3GENICheterozygous50572257
124248502942485030GGT7GENICpossibly homozygous50572259
124248719442487195GA23GENIChomozygous50327513
124248845542488456C-15GENIChomozygous50327515
124249059342490594AG22GENIChomozygous50327517
124249059542490596A-22GENIChomozygous50327519
124249060342490609CACACA------22GENIChomozygous50327521
124249065742490658CT29GENIChomozygous50209180
124249123642491237A-16GENICpossibly homozygous50327525
124249291842492919CT23GENIChomozygous50327527
124249410142494102CA36INTERGENIChomozygous50209183