chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7102116171021162TG3GENIChomozygous108273180
X7102122771021228GA9GENIChomozygous108273182
X7104479971044800AT2GENIChomozygous108391207
X7104496471044965CT9GENIChomozygous108273188
X7104496571044966TC8GENIChomozygous108273190
X7104514671045147CG6GENIChomozygous108273196
X7104517371045174CG6GENIChomozygous108273198
X7104553071045531CT9GENIChomozygous108273202
X7104553571045536GA8GENIChomozygous108273204
X7104556171045562GC4GENIChomozygous108273206
X7104556871045569TA2GENIChomozygous108273208
X7104556971045570AT7GENIChomozygous108391209
X7104560871045609TC7GENIChomozygous108391211
X7104560971045610CA7GENIChomozygous108391213
X7105144371051444AC6GENIChomozygous108273210
X7105147671051477GA9GENIChomozygous108391215
X7105149471051495GA11GENIChomozygous108391217
X7105149771051498CA13GENIChomozygous108391219
X7105150671051507GA12GENIChomozygous108391221
X7105151071051511GA13GENIChomozygous108391223
X7105154671051547GA8GENIChomozygous108449787
X7105154771051548AG8GENIChomozygous108391225
X7105155771051558CT7GENIChomozygous108273212
X7107956971079570CA11GENIChomozygous108596362
X7107957671079577CT13GENIChomozygous108501755
X7107958371079584GT13GENIChomozygous108501757