chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141763979717639798AT18GENIChomozygous980250615
141763983717639838GC15GENIChomozygous980250616
141763993717639938GA37GENIChomozygous980250617
141763996417639965AG43GENIChomozygous980250618
141764015017640151CG46GENIChomozygous980250619
141764052717640528GT36GENIChomozygous980250620
141764053317640534GA36GENIChomozygous980250621
141764171317641714CT73GENICpossibly homozygous980250622
141764266917642670AG37GENIChomozygous980250623
141764287317642874GT63GENIChomozygous980250624
141764307417643075CT38GENIChomozygous980250625
141764414917644150CA23GENIChomozygous980250626
141764869017648691GC44GENIChomozygous980250627
141764987017649871CA25GENIChomozygous980250628
141765004317650044CT24GENIChomozygous980250629
141765048617650487CT26GENIChomozygous980250630
141765054617650547TC57GENIChomozygous980250631
141765054917650550CT60GENIChomozygous980250632
141765055317650554GA65GENIChomozygous980250633
141765061417650615CT65GENIChomozygous980250634
141765064217650643AT51GENICpossibly homozygous980250635
141765064417650645AT49GENICpossibly homozygous980250636
141765067217650673TG52GENIChomozygous980250637
141765072117650722AG43GENIChomozygous980250638
141765073017650731CT40GENIChomozygous980250639
141765115717651158AT4GENIChomozygous980250640
141765116317651164GA6GENIChomozygous980250641
141765141217651413AT10GENIChomozygous980250642
141765144717651448TG9GENIChomozygous980250643
141765161617651617AG56GENIChomozygous980250644
141765171117651712GC45GENIChomozygous980250645
141765171817651719GA41GENIChomozygous980250646
141765172617651727GT45GENIChomozygous980250647
141765179617651797GA42GENIChomozygous980250648
141765415917654160CT28GENIChomozygous980250649
141765416217654163AG28GENIChomozygous980250650
141765581617655817TC31GENIChomozygous980250651
141765645617656457TC37GENIChomozygous980250652
141765685017656851AG21GENIChomozygous980250653