chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189829637189829638AG49GENIChomozygous793013386
2189829929189829930TC39GENIChomozygous793013387
2189829990189829991CT35GENIChomozygous793013388
2189830864189830865AG22GENIChomozygous793013389
2189831648189831649CA46GENIChomozygous793013390
2189832666189832667GA38GENIChomozygous793013391
2189832888189832889GA30GENICheterozygous793013392
2189833106189833107TA169GENICheterozygous793013393
2189833110189833111GT161GENICheterozygous793013394
2189833916189833917AC36GENIChomozygous793013395
2189834736189834737AG34GENICpossibly homozygous793013396
2189835091189835092TA50GENIChomozygous793013397