chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X123900994123900995AG5GENIChomozygous984022981
X123901333123901334TC6GENIChomozygous984022982
X123901666123901667CA6GENIChomozygous984022983
X123902771123902772CT8GENIChomozygous984022984
X123903040123903041CT15GENIChomozygous984022985
X123903719123903720TA10GENIChomozygous984022986
X123905627123905628AG4GENIChomozygous984022987
X123906932123906933TA8GENIChomozygous984022988
X123907599123907600CT10GENIChomozygous984022989
X123909136123909137CG7GENIChomozygous984022990
X123911461123911462GT11INTERGENIChomozygous984022991
X123911482123911483GA13INTERGENIChomozygous984022992
X123911483123911484TG14INTERGENIChomozygous984022993
X123912197123912198TC15INTERGENIChomozygous984022994
X123914613123914614AG6INTERGENIChomozygous984022995
X123916196123916197AG12INTERGENIChomozygous984022996
X123916552123916553GA11INTERGENIChomozygous984022997
X123916936123916937AG5INTERGENIChomozygous984022998