chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171188766011887661GGA28GENICpossibly homozygous47021193
171188942911889430GT47GENIChomozygous47366159
171188968211889683AC51GENIChomozygous47366161
171189023411890235AG56GENIChomozygous47021195
171189036611890367CG48GENIChomozygous47021196
171189108711891088CA60GENIChomozygous47366163
171189180811891812AAAC----14GENIChomozygous47366165
171189189611891897CA17GENICpossibly homozygous47366167
171189190611891908AA--15GENICpossibly homozygous47021206
171189190711891908A-15GENICheterozygous47021207
171189219311892194AG47GENICpossibly homozygous47021208
171189308111893082G-21GENIChomozygous47021209
171189349811893499GT32GENIChomozygous47366169
171189424211894243C-5GENICheterozygous47021210
171189569011895691GT44GENIChomozygous47366171
171189595711895958TC49GENIChomozygous47021211
171189599711895998G-40GENIChomozygous47366173
171189671411896715AG61GENIChomozygous47021213
171189882811898829CT46GENICpossibly homozygous47366175
171190051811900519GA61GENIChomozygous47366177
171190083711900838CT42GENIChomozygous47366179
171190115811901159AT27GENICheterozygous47582902