chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37762274677622747G16GENIChomozygous140868519
37762275477622755GT13GENICheterozygous403069114
37762275477622755G13GENIChomozygous403069115
37762487177624872TC48GENIChomozygous136756056
37762548577625486GA56GENICpossibly homozygous136756058
37762327877623279CT48GENIChomozygous136756054
37762377777623778TC34GENIChomozygous136756055
37762535877625359GT52GENIChomozygous136756057
37762364277623756AAGATCCAGGACTCGGGGTTGGGGATTTAGCTCAGCGGTAGAGCACTTGCCTAGCAAGCACAAGGCCCTGGGTTCGGTCCCCAGCTCTGAAGAAAAAAGAAAAAAAAAAAAAAA28GENIChomozygous136574390
37762554177625542CT61GENIChomozygous136756059
37762762077627621CG49GENIChomozygous136756060
37762892577628926GT67GENIChomozygous136756061
37762927477629275CT69GENIChomozygous136756062
37762958277629583CA55GENIChomozygous136756063
37763099577630996TC58GENIChomozygous136756064
37763117577631176CT60GENIChomozygous136756065
37763118277631186CAGA60GENIChomozygous136574391
37763196977631970AG66GENIChomozygous136756066
37763226677632267GA55GENIChomozygous136756067
37763231477632315GA64GENIChomozygous136756068
37763403977634040TC58GENIChomozygous136756069
37763414677634147AG27GENICpossibly homozygous136756070
37763423377634234TC56GENICpossibly homozygous136756071
37763427677634277TC56GENICpossibly homozygous136756072
37763440577634411TAGCTT56GENICpossibly homozygous136574392
37763455277634553TC53GENIChomozygous136756073
37763576577635790ACCACACAGACACACATCACACACA16GENIChomozygous136574393
37763611877636119CT21GENIChomozygous136756074
37763639477636395AG42GENIChomozygous136756075
37763851477638515AC46GENIChomozygous136756076
37763863677638636C31GENIChomozygous136574394
37764031477640315GC48GENIChomozygous136756077
37764041577640416TC41GENIChomozygous136756078
37764088177640882GA50GENIChomozygous136756079
37764147877641479CT71GENIChomozygous136756080