chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4135416073135416074GC28INTERGENIChomozygous72507216
4135416406135416407TC27INTERGENIChomozygous71157490
4135416775135416776GA30INTERGENIChomozygous72507218
4135416983135416984GC32INTERGENIChomozygous72507220
4135417011135417012TG28INTERGENIChomozygous71157499
4135418072135418073CA12INTERGENIChomozygous71157511
4135418113135418114AG16INTERGENIChomozygous71157514
4135418284135418285GT29INTERGENIChomozygous71157517
4135418394135418395AC15INTERGENIChomozygous71157520
4135418701135418702CG15INTERGENIChomozygous71157529
4135419602135419603CT3INTERGENIChomozygous72507222
4135419606135419607CT2INTERGENIChomozygous72507224
4135419881135419882GA29INTERGENIChomozygous72507226
4135420092135420093CT20INTERGENICpossibly homozygous72507228
4135420235135420236GA27INTERGENIChomozygous72507230
4135420800135420801AG25INTERGENIChomozygous71157550