chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71150144411501445GA5GENIChomozygous893055175
71150349111503492GA8GENIChomozygous893055176
71150392711503928AC4GENIChomozygous893055177
71150394111503942TC5GENIChomozygous893055178
71150442211504423CA6GENIChomozygous893055179
71150510211505103AG12GENIChomozygous893055180
71150534411505345AC13GENIChomozygous893055181
71150538811505389CT7GENIChomozygous893055182
71150540111505402CT7GENIChomozygous893055183
71150550111505502CT5GENIChomozygous893055184
71150559611505597CT6GENIChomozygous893055185
71150645011506451GA14GENIChomozygous893055186
71150682711506828AG12GENIChomozygous893055187
71150741711507418GA10GENIChomozygous893055188
71150743211507433TC6GENIChomozygous893055189
71150781711507818TC14GENIChomozygous893055190
71150783711507838GA9GENIChomozygous893055191
71150786811507869CT15GENIChomozygous893055192
71150854311508544TG14GENIChomozygous893055193
71150891111508912CT10GENIChomozygous893055194
71150920611509207GA8GENIChomozygous893055195
71150969911509700AC9GENIChomozygous893055196
71150992511509926AG13GENIChomozygous893055197
71151030511510306CT4GENIChomozygous893055198
71151078411510785GA4GENIChomozygous893055199
71151080711510808CT10GENIChomozygous893055200
71151113711511138TC9GENIChomozygous893055201
71151148011511481GA12GENIChomozygous893055202
71151176211511763GA16GENIChomozygous893055203
71151204611512047TC17GENIChomozygous893055204
71151214411512145GA8GENIChomozygous893055205
71151215911512160TC6GENIChomozygous893055206
71151247511512476TC15GENIChomozygous893055207
71151271411512715GC4GENIChomozygous893055208
71151290311512904AC9GENIChomozygous893055209