chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4135416073135416074GC31INTERGENICpossibly homozygous72507216
4135416406135416407TC24INTERGENIChomozygous71157490
4135416707135416708AG16INTERGENIChomozygous71157496
4135416775135416776GA14INTERGENIChomozygous72507218
4135416983135416984GC30INTERGENIChomozygous72507220
4135417011135417012TG42INTERGENIChomozygous71157499
4135418072135418073CA16INTERGENICpossibly homozygous71157511
4135418113135418114AG19INTERGENIChomozygous71157514
4135418284135418285GT24INTERGENIChomozygous71157517
4135418394135418395AC19INTERGENIChomozygous71157520
4135418667135418668AG11INTERGENIChomozygous71157523
4135418701135418702CG16INTERGENIChomozygous71157529
4135419881135419882GA33INTERGENIChomozygous72507226
4135420092135420093CT19INTERGENICpossibly homozygous72507228
4135420235135420236GA21INTERGENICpossibly homozygous72507230
4135420800135420801AG14INTERGENICpossibly homozygous71157550
4135418632135418633GA18INTERGENIChomozygous73915194