chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2169311221693113T-1GENIChomozygous45104190
X2169835221698353GA9GENIChomozygous45104192
X2170200121702002CT4GENIChomozygous45104193
X2170200421702005A-4GENIChomozygous45104194
X2170657921706580AG19GENIChomozygous45104195
X2170859521708596GA2GENIChomozygous45104196
X2170861421708615GA6GENICheterozygous45104197
X2170925021709251AACC1GENIChomozygous45104198
X2171201521712016AC8GENICheterozygous45104203
X2171401321714014CT10GENICpossibly homozygous45104204
X2171672021716721TTA1GENIChomozygous45104208
X2172600921726010GC19GENICpossibly homozygous45104211
X2172630621726307CG14GENIChomozygous45104212
X2172655821726559GA22GENICpossibly homozygous45104213
X2172728921727290CCTT2GENIChomozygous45104215
X2172999121729992TTA1GENIChomozygous45104222
X2173071821730719CCAA1GENIChomozygous45474528
X2173183321731835AA--4GENIChomozygous45104224
X2173205421732055GGA4GENIChomozygous45104225
X2173551121735512CCCA4GENIChomozygous45104229
X2173573821735739GGA1GENIChomozygous45474530