chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5137720702137720703TC12GENIChomozygous55745546
5137720902137720903CT25GENIChomozygous55745547
5137722895137722896AG15GENIChomozygous55745548
5137723707137723708GA22GENIChomozygous55901535
5137724507137724508TC27GENIChomozygous55901536
5137725462137725463TC23GENIChomozygous55745550
5137727036137727037AACAG41GENICheterozygous55901541
5137727113137727127CACCTCAGACCTTT--------------38GENICheterozygous56456931
5137727129137727130T-31GENICheterozygous56456932
5137728614137728626GCACCTGCACCC------------9GENIChomozygous55745554
5137729882137729896TGTGTGTGTGTGTG--------------4GENIChomozygous56456934
5137736720137736721GA17GENIChomozygous55901542
5137737878137737879AT25GENIChomozygous55901544
5137738264137738265CA30GENICpossibly homozygous55901546
5137738355137738356TC23GENIChomozygous55745559
5137738751137738752TC9GENIChomozygous55745560
5137740777137740778AG20GENIChomozygous55745561
5137740778137740779AG19GENIChomozygous55745562
5137740779137740780TTTG20GENIChomozygous55745563
5137741017137741018AAGTGTGTGT3GENIChomozygous56456935
5137741713137741714AG25GENIChomozygous55901547
5137742270137742271AC25GENIChomozygous55745567
5137743760137743771ACCTAGGCTGG-----------19GENIChomozygous55901549
5137747151137747152AG12GENIChomozygous55901550
5137747477137747478TA24GENICpossibly homozygous55901553
5137749406137749412AGAGAG------2GENIChomozygous56456936
5137749790137749794ACAC----3GENIChomozygous56456937
5137750023137750024AAT14GENICheterozygous55745572
5137750023137750024AATT14GENICpossibly homozygous55901555