chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8106845394106845395AT48GENIChomozygous138409184
8106848010106848011TC36GENIChomozygous138409189
8106848712106848713GA32GENIChomozygous138409190
8106849882106849883AG27GENIChomozygous142098967
8106850072106850073GA9GENIChomozygous142098968
8106850107106850108GA10GENIChomozygous142098969
8106850117106850118TC7GENIChomozygous142098970
8106850152106850153AG7GENIChomozygous142098971
8106850189106850191TG13GENIChomozygous142030124
8106850372106850373AG17GENIChomozygous138409192
8106850397106850398AT22GENIChomozygous142098972
8106850530106850531TG32GENIChomozygous142098973
8106850591106850592GA30GENIChomozygous142098974
8106850659106850660TG36GENIChomozygous138409193
8106850666106850667GT36GENIChomozygous142098975
8106850789106850790TC38GENIChomozygous142098976
8106852098106852099AT26GENIChomozygous142098979
8106852243106852244TC27GENIChomozygous142098980
8106852284106852284GAA25GENIChomozygous142030125
8106853057106853058GA48GENIChomozygous142098981
8106853600106853601TA56GENIChomozygous138409194
8106854335106854336CT42GENIChomozygous138409195
8106856848106856849AT40GENICpossibly homozygous138409196
8106848822106848823CA27GENIChomozygous145673774
8106853282106853283TA47GENIChomozygous145673775
8106853238106853238TAA38GENICpossibly homozygous138263079