chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5173153122173153123TC11GENIChomozygous114094353
5173158113173158114GA7GENIChomozygous114094355
5173163525173163526AC26GENIChomozygous114094359
5173163861173163862AG14GENIChomozygous114094361
5173163949173163950TG13GENIChomozygous114094363
5173164173173164174GA5GENIChomozygous114094365
5173164175173164176TC6GENIChomozygous114094367
5173164310173164311TA5GENIChomozygous114094369
5173164364173164365AG18GENIChomozygous114094371
5173164546173164547TG17GENIChomozygous114094373
5173164630173164631AG23GENIChomozygous114094375
5173165694173165695TC22GENIChomozygous114094377
5173167259173167260GA21GENIChomozygous114094379
5173171985173171986GC20GENIChomozygous114094383
5173173052173173053AT12GENIChomozygous114094385
5173175238173175239CT19GENIChomozygous114094387
5173175967173175968AG21GENIChomozygous114094389
5173177185173177186TA19GENIChomozygous114094391
5173177689173177690CT19GENIChomozygous114094393
5173177815173177816GT30GENIChomozygous114094395
5173178142173178143TC12GENIChomozygous114094397
5173180393173180394GA25GENIChomozygous114094399
5173181070173181071TG15GENIChomozygous114094401