chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106753329767533298CT24GENIChomozygous116795741
106753479767534798GC17GENIChomozygous116942571
106753770167537702GT29GENIChomozygous116795745
106753778667537787TC38GENICpossibly homozygous116795747
106753811367538114GA35GENIChomozygous116795749
106753816667538167GT32GENIChomozygous116795751
106753818167538182TC25GENIChomozygous116795753
106753902467539025AG19GENIChomozygous116942573
106753932267539323TC24GENIChomozygous116795755
106753934267539343GA30GENIChomozygous116795757
106753995167539952GA33GENIChomozygous116795759
106754052267540523GA32GENICpossibly homozygous116795761
106754090367540904AG21GENIChomozygous116795765
106754185267541853TC12GENIChomozygous116942577
106754214067542141GA35GENIChomozygous116795767
106754219167542192AG35GENIChomozygous116795769
106754273467542735AG22GENIChomozygous116795771
106754322567543226TC10GENIChomozygous116795773
106754353667543537CA24GENICpossibly homozygous116795775
106754370367543704GA27GENIChomozygous116795777
106754416067544161GA30GENIChomozygous116795779
106754419867544199AG25GENIChomozygous116795781
106754420467544205AG24GENIChomozygous116795783
106754426467544265AG24GENIChomozygous116795785
106754450767544508GA32GENIChomozygous116795787
106754453167544532AG39GENIChomozygous116795789
106754453267544533AG38GENIChomozygous116795791
106754460267544603CA31GENIChomozygous116795793
106754464067544641GC29GENIChomozygous116795795
106754583367545834TG36GENIChomozygous116795801
106754593067545931CT24GENIChomozygous116795803
106754611767546118GA27GENIChomozygous116795805
106754652567546526TC11GENIChomozygous116795807
106754677567546776TC28GENIChomozygous116795809
106754700367547004AG27GENICpossibly homozygous116795811
106754718267547183CT33GENICpossibly homozygous116795813
106754769167547692GC15GENIChomozygous116795815
106754770867547709CT19GENIChomozygous116795817
106754803567548036TC26GENIChomozygous116795819
106755009067550091AG32GENIChomozygous116795821
106755104667551047CT32GENIChomozygous116795823