chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141763972417639725TC32GENIChomozygous930237767
141764052517640526TC36GENIChomozygous930237768
141764074817640749AG51GENIChomozygous930237769
141764103217641033CT40GENIChomozygous930237770
141764199917642000GA42GENIChomozygous930237771
141764239717642398GT45GENIChomozygous930237772
141764280717642808TC37GENIChomozygous930237773
141764307417643075CT40GENIChomozygous930237774
141764869017648691GC38GENIChomozygous930237775
141765040117650402TC20GENIChomozygous930237776
141765048617650487CT18GENIChomozygous930237777
141765054617650547TC29GENICpossibly homozygous930237778
141765054917650550CT29GENICpossibly homozygous930237779
141765055317650554GA29GENICpossibly homozygous930237780
141765061417650615CT39GENICpossibly homozygous930237781
141765064217650643AT40GENICpossibly homozygous930237782
141765064417650645AT43GENICpossibly homozygous930237783
141765067217650673TG31GENICpossibly homozygous930237784
141765072117650722AG27GENIChomozygous930237785
141765073017650731CT27GENIChomozygous930237786
141765112317651124TA12GENIChomozygous930237787
141765115717651158AT25GENIChomozygous930237788
141765116317651164GA27GENIChomozygous930237789
141765141217651413AT24GENIChomozygous930237790
141765144717651448TG28GENIChomozygous930237791
141765161617651617AG55GENIChomozygous930237792
141765171117651712GC38GENIChomozygous930237793
141765171817651719GA34GENIChomozygous930237794
141765172617651727GT36GENIChomozygous930237795
141765179617651797GA36GENIChomozygous930237796
141765415917654160CT43GENIChomozygous930237797
141765416217654163AG43GENIChomozygous930237798
141765438217654383CA32GENIChomozygous930237799
141765581617655817TC24GENIChomozygous930237800
141765617717656178TG39GENIChomozygous930237801
141765645617656457TC39GENIChomozygous930237802
141765685017656851AG30GENIChomozygous930237803