chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2187741780187741781GC34INTERGENIChomozygous59293582
2187741861187741862CT43INTERGENIChomozygous60225719
2187742072187742073TC28INTERGENIChomozygous59293586
2187742217187742218TA18INTERGENIChomozygous60225720
2187742536187742537AC14INTERGENIChomozygous60225721
2187742868187742869AATG5INTERGENICheterozygous61759613
2187742880187742881AATG3INTERGENICheterozygous61759615
2187742899187742900GC10INTERGENIChomozygous59768979
2187743188187743189CT29INTERGENIChomozygous59293593
2187743229187743230AG28INTERGENIChomozygous60225722
2187743501187743502GA21INTERGENIChomozygous59293595
2187744280187744281TTA16INTERGENIChomozygous60225723
2187745518187745519AG26INTERGENIChomozygous60225724
2187745603187745604GA21INTERGENIChomozygous59293603
2187745841187745842TA14INTERGENICpossibly homozygous60894455
2187745926187745927TC18INTERGENIChomozygous60225725
2187746274187746275GC13INTERGENICpossibly homozygous60225726
2187746895187746896CT19INTERGENICpossibly homozygous60225727
2187746929187746930GA20INTERGENIChomozygous59293608
2187746973187746974GGA15INTERGENIChomozygous60225728