chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121309164213091643AG49GENIChomozygous115259742
121309229913092300GT44GENICpossibly homozygous115259744
121309251213092513GA35GENIChomozygous115259746
121309275513092756TA26GENIChomozygous115259748
121309670013096701GA30GENIChomozygous115259750
121309821013098211GC32GENIChomozygous115259752
121309965013099651TC40GENIChomozygous115259754
121310247313102474TC37GENIChomozygous115259756
121310367613103677CT36GENIChomozygous115259758
121310384413103845AT61GENIChomozygous115259760
121310428113104282GA35GENIChomozygous115259762
121310534813105349CT27GENIChomozygous115416645
121310556513105566TG48GENIChomozygous115259764
121310570713105708CG33GENIChomozygous115259766
121310718213107183CT47GENIChomozygous115259768
121310764013107641CT34GENIChomozygous115259770
121310921113109212CT34GENIChomozygous115259772
121310931613109317GA44GENIChomozygous115259774
121311069513110696TC44GENIChomozygous115259776
121311174813111749AG45GENIChomozygous115416647