chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1768127917681280TA10GENIChomozygous62915985
X1768256317682564CG18GENIChomozygous62915986
X1768335117683352GA15GENIChomozygous62915987
X1768689217686893AT16GENIChomozygous62915988
X1769069417690695TC10GENIChomozygous62915989
X1769547917695480AG15GENIChomozygous62915990
X1770056217700563T21GENICpossibly homozygous63167892
X1770071017700711G8GENIChomozygous63167893
X1770145817701459AT9GENIChomozygous62915991
X1770183517701836AT5GENIChomozygous62915992
X1770270717702708AT6GENIChomozygous62915993
X1770360717703612GTATG15GENICheterozygous63167894
X1770745317707454GC4GENIChomozygous63136568
X1771370817713709GA12GENIChomozygous62916000
X1771385717713858T18GENICheterozygous63167895
X1772294117722942CT9GENIChomozygous62916001
X1772466317724664CT4GENIChomozygous62916002
X1773243717732438C15GENICheterozygous63167896
X1770742617707427CA4GENIChomozygous63206077