chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187139689271396893GA16GENIChomozygous110498343
187139828571398286CT25GENIChomozygous110498345
187139828671398287CT26GENIChomozygous110498347
187139931671399317GA26GENIChomozygous110396634
187139972171399722CT22GENIChomozygous110732826
187140171171401712TG32GENICpossibly homozygous110396636
187140566271405663AC35GENIChomozygous110396638
187140578371405784AG27GENIChomozygous110396640
187140621371406214CT29GENIChomozygous110498351
187140702971407030CG31GENIChomozygous110396642
187140820971408210AG37GENIChomozygous110396644
187140836571408366TC37GENIChomozygous110396646
187140871671408717CG35GENIChomozygous110396648
187140876871408769AG31GENICpossibly homozygous110396650
187140911571409116CT28GENIChomozygous110498353
187141021771410218AG31GENIChomozygous110396652
187141125571411256GA12GENIChomozygous110498355
187141171871411719CT23GENIChomozygous110498357
187141190571411906CT41GENIChomozygous110498359
187141200071412001CT38GENIChomozygous110498361
187141202171412022CT35GENIChomozygous110396659
187141232671412327CT22GENIChomozygous110498363
187141234371412344CA21GENIChomozygous110498365
187141244971412450GT24GENIChomozygous110498367
187141313671413137GA11GENIChomozygous110396663
187141377071413771AG16GENIChomozygous110396665
187141490171414902GA11GENIChomozygous110498369
187141536471415365GA23GENIChomozygous110498371
187141591271415913TC42GENIChomozygous110396667
187141596571415966GC41GENIChomozygous110396669
187141662871416629GA27GENIChomozygous110396671
187141694371416944TG29GENIChomozygous110396673
187141697271416973CT31GENIChomozygous110396675
187141716671417167AT40GENIChomozygous110498373
187141763471417635AC32GENIChomozygous110396677
187141904471419045AG27GENIChomozygous110396683
187141906071419061CT26GENIChomozygous110498375
187141913071419131TC23GENIChomozygous110396685
187142186371421864CT27GENIChomozygous110498377
187142191571421916GA24GENIChomozygous110498379