chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125184766151847662TC16GENIChomozygous115355672
125184861451848615TC18GENIChomozygous115355673
125184900051849001TC23GENIChomozygous115355674
125184906851849069TC26GENIChomozygous115355675
125185053251850533AG14GENIChomozygous115355676
125185297151852972AG8GENIChomozygous115355677
125185304451853045TA16GENIChomozygous115355678
125185405051854051TC23GENIChomozygous115355679
125185664051856641TC17GENIChomozygous115355680
125185686851856869TC16GENIChomozygous115355681
125185778351857784GA20GENIChomozygous115355682
125185934351859344GT19GENIChomozygous115355683
125186039051860391GA21GENIChomozygous115355684
125186092351860924TC13GENIChomozygous115355685
125186179851861799AG17GENIChomozygous115355687
125186205451862055AC22GENIChomozygous115355688
125186278951862790GA17GENIChomozygous115355689
125186280051862801GT19GENIChomozygous115355690
125186317751863178TC25GENIChomozygous115355691
125186469251864693CT18GENIChomozygous115355692
125186561351865614CA7GENIChomozygous115355693
125186797551867976CT14GENIChomozygous115355695
125186903351869034CT22GENIChomozygous115355696
125186955951869560GA21GENIChomozygous115355697
125187011051870111CT11GENIChomozygous115355698
125187152351871524GA17GENIChomozygous115355699
125187304751873048GA18GENIChomozygous115404432
125187499551874996CA13GENIChomozygous115355700
125187499651874997CA13GENIChomozygous115355701
125187501051875011TG15GENIChomozygous115355702
125187601251876013TC15GENIChomozygous115355703
125187651751876518TC14GENIChomozygous115355704
125187694651876947GC15GENIChomozygous115355705
125187701151877012CT18GENIChomozygous115355706
125187799851877999GC9GENIChomozygous115355707