chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5173153122173153123TC37GENIChomozygous114094353
5173163525173163526AC36GENIChomozygous114094359
5173163861173163862AG24GENIChomozygous114094361
5173163949173163950TG14GENIChomozygous114094363
5173164173173164174GA17GENIChomozygous114094365
5173164175173164176TC16GENIChomozygous114094367
5173164310173164311TA23GENIChomozygous114094369
5173164364173164365AG25GENIChomozygous114094371
5173164546173164547TG28GENIChomozygous114094373
5173164630173164631AG30GENIChomozygous114094375
5173165694173165695TC25GENIChomozygous114094377
5173167259173167260GA26GENIChomozygous114094379
5173170549173170550AG8GENICheterozygous119064741
5173171985173171986GC30GENIChomozygous114094383
5173173052173173053AT21GENIChomozygous114094385
5173175238173175239CT25GENIChomozygous114094387
5173175967173175968AG26GENIChomozygous114094389
5173177185173177186TA26GENIChomozygous114094391
5173177689173177690CT33GENIChomozygous114094393
5173177815173177816GT33GENIChomozygous114094395
5173178142173178143TC28GENIChomozygous114094397
5173180393173180394GA38GENIChomozygous114094399
5173181070173181071TG27GENIChomozygous114094401