chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5111793808111793809C-21GENIChomozygous55640392
5111794578111794579TC27GENIChomozygous55640393
5111794930111794931TC9GENIChomozygous56051902
5111795796111795797CCTCTCT3GENIChomozygous56051905
5111796184111796185AG28GENIChomozygous56051906
5111796349111796350TC23GENIChomozygous56333348
5111796930111796931GC28GENIChomozygous56051907
5111797194111797195CCAA8GENIChomozygous56051908
5111799601111799605GAGG----8GENICpossibly homozygous56445281
5111799957111799958CCT5GENIChomozygous55640401
5111799974111799980GGGGGT------3GENIChomozygous56051909
5111800143111800151CTTTCTTC--------6GENIChomozygous56445283
5111800171111800172CT7GENIChomozygous56051911
5111800267111800268TC17GENIChomozygous56051912
5111800816111800817GT19GENIChomozygous56051913
5111800925111800926CG7GENIChomozygous56445285
5111800927111800940GCAGCAGCAGCAG-------------6GENIChomozygous56445287
5111801191111801192TC15GENIChomozygous56051915