chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7101180971011810TG2GENIChomozygous108449769
X7102082971020830AC5GENIChomozygous108391199
X7102083771020838AT5GENIChomozygous108391201
X7102084171020842AC4GENIChomozygous108391203
X7102097071020971GT11GENIChomozygous108391205
X7102083671020837GC5GENIChomozygous108732753
X7102087371020874GA11GENIChomozygous108732755
X7102088371020884GT10GENIChomozygous108526534
X7102091271020913CA13GENIChomozygous108619825
X7102091471020915AG11GENIChomozygous108501753
X7102116171021162TG13GENIChomozygous108273180
X7104505471045055CA13GENIChomozygous108273192
X7104505571045056AC13GENIChomozygous108273194
X7104514671045147CG14GENIChomozygous108273196
X7104517371045174CG9GENIChomozygous108273198
X7104530471045305GT8GENIChomozygous108273200
X7104556171045562GC5GENIChomozygous108273206
X7104556871045569TA5GENIChomozygous108273208
X7104556971045570AT5GENIChomozygous108391209
X7105147671051477GA6GENIChomozygous108391215
X7105149471051495GA5GENIChomozygous108391217
X7105149771051498CA5GENIChomozygous108391219
X7105150671051507GA6GENIChomozygous108391221
X7105151071051511GA5GENIChomozygous108391223
X7105154671051547GA7GENIChomozygous108449787
X7105154771051548AG7GENIChomozygous108391225
X7105155771051558CT9GENIChomozygous108273212
X7107240571072406AC14GENIChomozygous108677228
X7107957671079577CT9GENIChomozygous108501755
X7107958371079584GT8GENIChomozygous108501757