chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31577221915772220AT9GENIChomozygous132046134
31577224815772249GC14GENIChomozygous132046135
31577225415772255TC13GENIChomozygous132046136
31577227515772276AC13GENIChomozygous132046137
31577228615772287AC13GENIChomozygous132046138
31577243615772437GC8GENIChomozygous112068454
31577245015772451TA8GENIChomozygous112068456
31577246315772464CA8GENIChomozygous132046139
31577264715772648AC11GENIChomozygous132046140
31577287815772879CT14GENIChomozygous125886814
31577288515772889CGTC13GENIChomozygous130900853
31577292515772926CG14GENIChomozygous132046141
31577301015773011GT12GENIChomozygous112068460
31577304715773048CT15GENIChomozygous125886815
31577318615773187CT20GENIChomozygous125886816
31577378915773790TG7GENIChomozygous132046142
31577385915773860TA6GENIChomozygous132046143
31577386415773865TC8GENIChomozygous132046144
31577408415774085AG6GENIChomozygous132046145
31577452915774530AG13GENICpossibly homozygous132046146
31577466915774669T12GENICpossibly homozygous132039078