chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101484803514848036T-34INTERGENIChomozygous51623758
101484815514848156CT39INTERGENICpossibly homozygous51623759
101484821014848211CCA27INTERGENIChomozygous51623760
101484821214848213CCT27INTERGENIChomozygous51623761
101484831914848320TG38INTERGENICpossibly homozygous51330211
101484834014848341CT32INTERGENICpossibly homozygous51623762
101484864014848641AG37INTERGENICpossibly homozygous51330214
101484878314848784AG29INTERGENIChomozygous51330216
101484884814848849GA27INTERGENIChomozygous51330218
101484936614849367TC32INTERGENIChomozygous51330219
101484946514849467CA--16INTERGENIChomozygous51623763
101484960514849606TA23INTERGENIChomozygous51330224
101484977714849778AAT11INTERGENIChomozygous51623764
101485061714850618AAGAGG14INTERGENIChomozygous51330237
101485201914852020GT32INTERGENICpossibly homozygous51330241
101485254414852545GC18INTERGENIChomozygous51330243
101485307014853071TG26INTERGENIChomozygous51330253
101485308414853085TG25INTERGENIChomozygous51330254
101485313314853134AG20INTERGENIChomozygous51330256
101485333814853339AG24INTERGENIChomozygous51330260
101485370814853709GC23INTERGENIChomozygous51623765
101484979114849792CCTTTTTT6INTERGENIChomozygous52481604
101485038514850395ACACACACAC----------3INTERGENIChomozygous52835182