chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5137720702137720703TC28GENIChomozygous55745546
5137720902137720903CT31GENIChomozygous55745547
5137722895137722896AG31GENICpossibly homozygous55745548
5137723707137723708GA23GENIChomozygous55901535
5137724507137724508TC25GENIChomozygous55901536
5137725462137725463TC22GENIChomozygous55745550
5137727036137727037AACAG41GENICheterozygous55901541
5137727113137727127CACCTCAGACCTTT--------------31GENICheterozygous56456931
5137728614137728626GCACCTGCACCC------------3GENIChomozygous55745554
5137736720137736721GA32GENIChomozygous55901542
5137737878137737879AT36GENIChomozygous55901544
5137738264137738265CA30GENIChomozygous55901546
5137738355137738356TC31GENIChomozygous55745559
5137738751137738752TC31GENIChomozygous55745560
5137740777137740778AG23GENIChomozygous55745561
5137740778137740779AG23GENIChomozygous55745562
5137740779137740780TTTG23GENIChomozygous55745563
5137741713137741714AG31GENIChomozygous55901547
5137742270137742271AC34GENIChomozygous55745567
5137743760137743771ACCTAGGCTGG-----------23GENIChomozygous55901549
5137747151137747152AG41GENIChomozygous55901550
5137747477137747478TA21GENIChomozygous55901553
5137750023137750024AAT20GENICheterozygous55745572
5137750023137750024AATT20GENICpossibly homozygous55901555