chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
39269530792695308AG32GENIChomozygous111656692
39269561992695620TC32GENIChomozygous111656694
39269616592696166GA17GENIChomozygous111656695
39269696392696964CT21GENIChomozygous111656697
39269850392698504GA21GENIChomozygous111656699
39270104092701041GA26GENIChomozygous111656701
39270121992701220CT38GENIChomozygous111656702
39270236992702370TC25GENIChomozygous111656703
39270272892702729TC21GENIChomozygous111656705
39270371292703713GC18GENIChomozygous111656711
39270399592703996AG22GENIChomozygous111656713
39270431692704317TA22GENIChomozygous111656715
39270449692704497AC25GENIChomozygous111656716
39270451992704520GA29GENIChomozygous111656718
39270645292706453AC25GENIChomozygous111656720
39270649092706491TC24GENIChomozygous111656722
39270652992706530AC28GENIChomozygous111656724
39270694492706945TA25GENIChomozygous111656725
39270720992707210TG26GENIChomozygous111656727
39270725392707254CT23GENIChomozygous111656729
39270757392707574AG25GENIChomozygous111656731
39270770892707709AG30GENIChomozygous111656733
39270831492708315AT35GENIChomozygous111656735
39270876892708769CT24GENIChomozygous111656737
39270898192708982GA26GENIChomozygous111656739
39270924292709243GA19GENIChomozygous111656741
39270930392709304GA8GENIChomozygous111656742
39270958192709582CG21GENIChomozygous111656746
39270959792709598AG20GENIChomozygous111656748
39270962692709627GC23GENIChomozygous111656750
39270977292709773AG19GENIChomozygous111656751
39271008892710089AC24GENIChomozygous111656753
39271066392710664AG29GENIChomozygous111656755
39271084792710848CA27GENIChomozygous111656757
39271090392710904GA28GENIChomozygous111656759
39271091092710911TA27GENIChomozygous111656761
39271167592711676CG33GENIChomozygous111656762
39271215192712152GA25GENIChomozygous111656764
39271426392714264TC36GENIChomozygous111656766
39271430292714303AG17GENIChomozygous111656768
39277916992779170AC27GENIChomozygous111955151
39278343392783434CT20GENIChomozygous119683236