chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
36421696364216964CT6GENIChomozygous58421253
36421701664217017GA17GENICpossibly homozygous58421254
36421707464217075AG13GENIChomozygous57405342
36421729864217299AG8GENIChomozygous57405348
36421764064217641TG11GENIChomozygous57405352
36421835164218352A-2GENIChomozygous57405359
36421846164218462AG3GENIChomozygous57405363
36421922964219230GC9GENIChomozygous57405364
36421940264219403GGA3GENICheterozygous57405366
36421940264219403GGAA3GENICheterozygous58806359
36421958364219584TC11GENIChomozygous57405368
36421959764219598TTG9GENICheterozygous57405370
36422005864220062GAAG----2GENICheterozygous57405382
36422033564220336AG18GENIChomozygous57405384
36422043664220437TC18GENIChomozygous57405386
36422104064221041GA22GENIChomozygous58421255
36422109064221091AG15GENIChomozygous57405388
36422122364221224TA7GENIChomozygous57405390
36422153864221539AT5GENIChomozygous57405392
36422161764221618TC2GENIChomozygous57405394
36422251064222511A-8GENICheterozygous57405397
36422311864223119TC8GENIChomozygous57405399
36422810164228102TC20GENICpossibly homozygous57405404
36422831064228311CT18GENIChomozygous58421256
36422845164228452AT25GENICpossibly homozygous57405406
36422875764228758CCG18GENICpossibly homozygous57405408
36422939764229398GA22GENIChomozygous58421257
36423123664231237GA10GENIChomozygous58421258
36423230164232302C-4GENIChomozygous58421259
36423418964234190TC16GENICpossibly homozygous57405427
36423691864236919TTA3GENICheterozygous57405442
36423825864238259CT1GENIChomozygous58421262
36423974864239749GT8GENIChomozygous58421263