chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8110220848110220849AG8GENIChomozygous138413351
8110221410110221411CT17GENIChomozygous138413352
8110222409110222410TC14GENIChomozygous138413353
8110222619110222620AT15GENIChomozygous138413354
8110222634110222635CT14GENIChomozygous138413355
8110223348110223348TCCT7GENIChomozygous138264322
8110223900110223901AG18GENIChomozygous138413356
8110227457110227458AG25GENIChomozygous138413362
8110224267110224268AG23GENIChomozygous138413357
8110224371110224372CA16GENIChomozygous138413358
8110225490110225491AG14GENIChomozygous138413359
8110226367110226368CT12GENIChomozygous138413360
8110227163110227164AC23GENIChomozygous138413361
8110229069110229070GT18GENIChomozygous138413363
8110229101110229102AG19GENIChomozygous138413364
8110229343110229344AG8GENIChomozygous138413365
8110229441110229441AA13GENIChomozygous138264325
8110230216110230217TC13GENIChomozygous138413366
8110230481110230482AG17GENIChomozygous138413367
8110232268110232284AACCATGCACACCTGT18GENIChomozygous138264326
8110232390110232391AG23GENIChomozygous138413368
8110232952110232953GA24GENIChomozygous138413369
8110234644110234645GT10GENIChomozygous138413370
8110229448110229449TA15GENIChomozygous154541840
8110229448110229449T15GENICheterozygous403248979