chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134864693648646936AAAC21GENIChomozygous131501691
134864802648648026C7GENIChomozygous129051761
134864804448648044C7GENIChomozygous129051762
134864796648647967C4GENIChomozygous129051759
134864798848647988G6GENIChomozygous129051760
134864805448648054C6GENIChomozygous129051763
134864806848648068A5GENIChomozygous129051764
134864807248648072C5GENIChomozygous129051765
134864809948648101CG4GENIChomozygous131501692
134864810448648119TGTGATACGGAATCC4GENIChomozygous131501693
134864814248648142A3GENIChomozygous129051766
134864817748648177A4GENIChomozygous131501694
134864820048648200G2GENIChomozygous131501695
134864826848648269A6GENIChomozygous131501696
134864831448648315T12GENIChomozygous129051768
134864832548648326G12GENIChomozygous129051769
134864924948649249A18GENIChomozygous131501697
134865014948650150GA18GENIChomozygous114549470
134864821748648218AC1GENIChomozygous118535362
134864825048648251GC2GENIChomozygous118450340
134864826948648270AT6GENIChomozygous131509541
134864893648648937CT16GENIChomozygous114549468
134864933048649331AG16GENIChomozygous114549469