chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141763979717639798AT22GENIChomozygous998314718
141763983717639838GC29GENIChomozygous998314719
141763993717639938GA25GENIChomozygous998314720
141763996417639965AG25GENIChomozygous998314721
141764000017640001CT29GENIChomozygous998314722
141764015017640151CG21GENIChomozygous998314723
141764052717640528GT36GENIChomozygous998314724
141764053317640534GA33GENIChomozygous998314725
141764171317641714CT21GENIChomozygous998314726
141764266917642670AG25GENIChomozygous998314727
141764287317642874GT28GENIChomozygous998314728
141764307417643075CT35GENIChomozygous998314729
141764414917644150CA31GENIChomozygous998314730
141764869017648691GC27GENIChomozygous998314731
141765004317650044CT17GENIChomozygous998314732
141765031617650317TC13GENIChomozygous998314733
141765040117650402TC12GENIChomozygous998314734
141765048617650487CT6GENIChomozygous998314735
141765054617650547TC15GENIChomozygous998314736
141765054917650550CT14GENIChomozygous998314737
141765055317650554GA15GENIChomozygous998314738
141765061417650615CT21GENIChomozygous998314739
141765064217650643AT20GENIChomozygous998314740
141765064417650645AT20GENIChomozygous998314741
141765067217650673TG22GENIChomozygous998314742
141765072117650722AG20GENIChomozygous998314743
141765073017650731CT19GENIChomozygous998314744
141765112317651124TA14GENIChomozygous998314745
141765115717651158AT21GENIChomozygous998314746
141765116317651164GA21GENIChomozygous998314747
141765141217651413AT30GENIChomozygous998314748
141765144717651448TG31GENIChomozygous998314749
141765161617651617AG23GENIChomozygous998314750
141765171117651712GC26GENIChomozygous998314751
141765171817651719GA24GENIChomozygous998314752
141765172617651727GT25GENIChomozygous998314753
141765179617651797GA15GENIChomozygous998314754
141765415917654160CT22GENIChomozygous998314755
141765416217654163AG23GENIChomozygous998314756
141765581617655817TC22GENIChomozygous998314757
141765645617656457TC23GENIChomozygous998314758
141765685017656851AG22GENIChomozygous998314759