chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157613853157613854GT13GENIChomozygous934916859
4157614185157614186TG22GENIChomozygous934916860
4157614774157614775AT26GENIChomozygous934916861
4157614977157614978AC23GENIChomozygous934916862
4157616535157616536CA22GENIChomozygous934916863
4157619978157619979GT13GENIChomozygous934916864
4157620744157620745TC34GENIChomozygous934916865
4157623083157623084GA27GENIChomozygous934916866
4157625710157625711CT23GENIChomozygous934916867
4157626447157626448TC16GENIChomozygous934916868
4157627043157627044TC22GENIChomozygous934916869
4157629525157629526TC34GENIChomozygous934916870
4157631950157631951AG23GENIChomozygous934916871
4157632657157632658TC33GENIChomozygous934916872
4157633500157633501AG8GENIChomozygous934916873
4157634098157634099TC31GENIChomozygous934916874
4157635239157635240AC24GENIChomozygous934916875
4157635295157635296CT19GENIChomozygous934916876
4157638495157638496TC23GENIChomozygous934916877
4157639657157639658GC24GENIChomozygous934916878
4157644216157644217CG13GENIChomozygous934916879
4157644340157644341TC26GENIChomozygous934916880