chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141763979717639798AT30GENIChomozygous945007064
141763983717639838GC36GENIChomozygous945007065
141763993717639938GA50GENIChomozygous945007066
141763996417639965AG40GENIChomozygous945007067
141764000017640001CT32GENIChomozygous945007068
141764015017640151CG38GENIChomozygous945007069
141764052717640528GT35GENIChomozygous945007070
141764053317640534GA31GENIChomozygous945007071
141764171317641714CT28GENIChomozygous945007072
141764266917642670AG18GENIChomozygous945007073
141764287317642874GT31GENIChomozygous945007074
141764307417643075CT32GENIChomozygous945007075
141764414917644150CA40GENIChomozygous945007076
141764869017648691GC37GENIChomozygous945007077
141764987017649871CA33GENIChomozygous945007078
141765072117650722AG32GENIChomozygous945007079
141765141217651413AT33GENIChomozygous945007080
141765144717651448TG39GENIChomozygous945007081
141765161617651617AG30GENIChomozygous945007082
141765172617651727GT31GENIChomozygous945007083
141765179617651797GA38GENIChomozygous945007084
141765438217654383CA25GENIChomozygous945007085
141765581617655817TC34GENIChomozygous945007086
141765645617656457TC19GENIChomozygous945007087
141765685017656851AG40GENIChomozygous945007088