chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7101180971011810TG3GENIChomozygous108449769
X7101181071011811CT3GENIChomozygous108449771
X7101181271011813AC3GENIChomozygous108449773
X7102097071020971GT14GENIChomozygous108391205
X7102091271020913CA12GENIChomozygous108619825
X7102091471020915AG12GENIChomozygous108501753
X7102111071021111CT8GENIChomozygous108619827
X7102111271021113TA8GENIChomozygous108619829
X7103589071035891CA2GENIChomozygous108619831
X7104485871044859TG2GENIChomozygous108619833
X7102116171021162TG9GENIChomozygous108273180
X7102122771021228GA8GENIChomozygous108273182
X7103589271035893CA1GENIChomozygous108570335
X7104505471045055CA8GENIChomozygous108273192
X7104505571045056AC8GENIChomozygous108273194
X7104514671045147CG10GENIChomozygous108273196
X7104553071045531CT6GENIChomozygous108273202
X7104553571045536GA4GENIChomozygous108273204
X7105144371051444AC10GENIChomozygous108273210
X7105147671051477GA8GENIChomozygous108391215
X7105149771051498CA11GENIChomozygous108391219
X7105150671051507GA12GENIChomozygous108391221
X7105151071051511GA12GENIChomozygous108391223
X7105154671051547GA7GENIChomozygous108449787
X7105154771051548AG7GENIChomozygous108391225
X7105155771051558CT9GENIChomozygous108273212
X7107957671079577CT8GENIChomozygous108501755
X7107958371079584GT8GENIChomozygous108501757