chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154493982744939828G21GENIChomozygous139632138
154493991144939912C29GENIChomozygous139632139
154494030744940307G41GENIChomozygous139632140
154494049444940495CA11GENICpossibly homozygous139726928
154494342544943426C23GENIChomozygous139632142
154494345844943459C26GENIChomozygous139632143
154494366344943664G46GENIChomozygous139632144
154494389244943893C35GENIChomozygous139632145
154494391544943915C37GENIChomozygous139632146
154494404044944041G45GENIChomozygous139632147
154494444544944446T33GENIChomozygous139632148
154494450644944507A22GENIChomozygous139632149
154494454144944542TC17GENIChomozygous139726929
154494454544944546TC18GENIChomozygous139726930
154494771744947718TA40GENIChomozygous139726931
154495011444950114G40GENIChomozygous139632152
154495014644950147G35GENIChomozygous139632153
154498081244980813TA15GENICheterozygous403381332
154498081244980813T15GENICheterozygous403381333
154498081444980815TA15GENICheterozygous403381334
154498081444980815T15GENICheterozygous403381335
154508846045088461A23GENICheterozygous403855558
154508846045088461AG23GENICheterozygous403855559
154511574945115750C16GENIChomozygous139632212