chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2314935623149357CT20GENIChomozygous125102094
X2314976723149768CT12GENIChomozygous125102095
X2315150123151502CT7GENIChomozygous125102096
X2315167523151676TC21GENIChomozygous125102097
X2315179923151800TA28GENIChomozygous125102098
X2315292723152928AG9GENIChomozygous125102099
X2315301623153017AG10GENIChomozygous125102100
X2315315223153153GA4GENIChomozygous125102101
X2315385123153852TG5GENIChomozygous125102102
X2315435423154355GA19GENIChomozygous125102103
X2315480923154810AG17GENIChomozygous125102104
X2315540523155406TA8GENIChomozygous125102105
X2316275323162754CT12GENIChomozygous125102106
X2316280223162803AG24GENIChomozygous125102107
X2316331623163317GT14GENIChomozygous125102108
X2316361523163616GA14GENIChomozygous125102109
X2316374323163744CT13GENIChomozygous125102110
X2316375623163757TC12GENIChomozygous125102111
X2316403523164036TC17GENIChomozygous125102112
X2316428623164287AG27GENIChomozygous125102113
X2316531423165315AG5GENIChomozygous125102114
X2316563123165632CA5GENIChomozygous125102115
X2315361123153612CT6GENIChomozygous125128988