chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154493982744939828G48GENIChomozygous139632138
154493991144939912C27GENIChomozygous139632139
154494030744940307G41GENIChomozygous139632140
154494049444940495CA13GENICheterozygous139726928
154494342544943426C25GENIChomozygous139632142
154494345844943459C25GENIChomozygous139632143
154494366344943664G51GENIChomozygous139632144
154494389244943893C35GENIChomozygous139632145
154494391544943915C31GENIChomozygous139632146
154494404044944041G49GENIChomozygous139632147
154494444544944446T26GENICpossibly homozygous139632148
154494450644944507A21GENIChomozygous139632149
154494454144944542TC27GENIChomozygous139726929
154494454544944546TC28GENIChomozygous139726930
154494771744947718TA32GENIChomozygous139726931
154495011444950114G68GENIChomozygous139632152
154495014644950147G63GENIChomozygous139632153
154500129145001292TC47GENIChomozygous144984384
154498081244980813TA23GENICheterozygous403381332
154498081244980813T23GENICpossibly homozygous403381333
154498081444980815TA23GENICheterozygous403381334
154498081444980815T23GENICpossibly homozygous403381335
154511574945115750C22GENICpossibly homozygous139632212
154511649045116491T23GENICheterozygous403381338
154504567945045680A7GENICheterozygous403381336
154504567945045680AT7GENICheterozygous403381337
154504568145045682A7GENICheterozygous403659070
154504568145045682AT7GENICheterozygous403659071
154511649045116491TG23GENICpossibly homozygous141121676