chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141763993717639938GA27GENICpossibly homozygous994945800
141763996417639965AG27GENICpossibly homozygous994945801
141764000017640001CT25GENICpossibly homozygous994945802
141764015017640151CG25GENICpossibly homozygous994945803
141764052717640528GT20GENIChomozygous994945804
141764053317640534GA18GENIChomozygous994945805
141764171317641714CT29GENICpossibly homozygous994945806
141764266917642670AG18GENIChomozygous994945807
141764287317642874GT16GENIChomozygous994945808
141764307417643075CT31GENIChomozygous994945809
141764414917644150CA20GENIChomozygous994945810
141764869017648691GC29GENIChomozygous994945811
141765054617650547TC13GENIChomozygous994945812
141765054917650550CT13GENIChomozygous994945813
141765055317650554GA10GENIChomozygous994945814
141765061417650615CT12GENIChomozygous994945815
141765064217650643AT12GENIChomozygous994945816
141765064417650645AT12GENIChomozygous994945817
141765072117650722AG17GENIChomozygous994945818
141765073017650731CT18GENIChomozygous994945819
141765112317651124TA6GENIChomozygous994945820
141765115717651158AT12GENIChomozygous994945821
141765116317651164GA13GENIChomozygous994945822
141765141217651413AT18GENIChomozygous994945823
141765144717651448TG17GENIChomozygous994945824
141765161617651617AG21GENIChomozygous994945825
141765171117651712GC20GENIChomozygous994945826
141765171817651719GA20GENIChomozygous994945827
141765172617651727GT16GENIChomozygous994945828
141765179617651797GA20GENIChomozygous994945829
141765415917654160CT19GENIChomozygous994945830
141765416217654163AG19GENIChomozygous994945831
141765438217654383CA25GENIChomozygous994945832
141765581617655817TC36GENIChomozygous994945833
141765645617656457TC19GENIChomozygous994945834
141765685017656851AG23GENIChomozygous994945835