chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5132274522132274523C-16GENIChomozygous56232684
5132274529132274530AG18GENIChomozygous56232685
5132274667132274668CG18GENIChomozygous56232687
5132275383132275384TC11GENIChomozygous55728555
5132276566132276567GC15GENIChomozygous56232688
5132276605132276606CCTTTTTTTTTTT6GENIChomozygous56452758
5132276635132276636AG15GENIChomozygous55728600
5132277262132277263CT27GENIChomozygous55728614
5132277599132277600AAGTGTGTTTGTGTGTGT6GENICheterozygous56569855
5132277599132277600AAGTGTGTTTGT6GENICheterozygous56531855
5132277599132277600AAGTGTGTTTGTGT6GENICheterozygous56531857
5132277771132277772TC23GENIChomozygous55728623
5132283967132283968CT19GENIChomozygous56232690
5132284045132284046TC26GENIChomozygous55728696
5132284756132284759TTT---17GENICpossibly homozygous56232691
5132285620132285621CCGTATGTAT8GENIChomozygous56531859
5132285757132285758TTACACACACACACACACACACAC9GENIChomozygous56452769
5132286660132286661AG38GENIChomozygous55728725
5132287600132287601GA15GENIChomozygous56354365
5132288237132288277TATATATATATATGTATATATATACACATATATACATATA----------------------------------------6GENIChomozygous56531861
5132287602132287603AACG9GENICheterozygous56551638