chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7816152078161521AG11GENIChomozygous108276133
X7816197578161976CT19GENIChomozygous108276135
X7816762578167626GA13GENIChomozygous108276138
X7816894178168942GA14GENIChomozygous108502192
X7816899178168992AT14GENIChomozygous108276140
X7816899278168993AT14GENIChomozygous108276142
X7817275778172758TC10GENIChomozygous108276144
X7818738978187390TC15GENIChomozygous108276146
X7818878278188783AT13GENIChomozygous108276150
X7818998678189987CT11GENIChomozygous108276154
X7819383078193831CT6GENIChomozygous108276156
X7819387078193871AC11GENIChomozygous108276158
X7819395378193954TA13GENIChomozygous108276160
X7819567178195672AC9GENIChomozygous108276164
X7819584778195848GT10GENIChomozygous108276166
X7819970778199708AC18GENIChomozygous108276168
X7819975878199759GT11GENIChomozygous108502194
X7820321678203217AT15GENIChomozygous108276172
X7820400878204009TC16GENIChomozygous108276174
X7820481478204815CT11GENIChomozygous108276176
X7820785278207853CG12GENIChomozygous108502195
X7820999678209997TG6GENIChomozygous108276180
X7821010878210109GA12GENIChomozygous108276182