chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145331103145331104TA31GENIChomozygous119315378
4145331478145331479TA26GENIChomozygous119315379
4145331564145331565CT22GENIChomozygous119315380
4145332229145332230GT28GENIChomozygous119315381
4145332717145332718CT29GENIChomozygous119315382
4145335071145335072A21GENICpossibly homozygous128087956
4145334010145334122AAGAAACCCAAAGAAGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAAAAAAAAAAAAA20GENIChomozygous132967613
4145334144145334146GC24GENIChomozygous132967614
4145334148145334151ACA24GENIChomozygous132967615
4145337437145337438AT20GENIChomozygous112870780
4145339285145339285G24GENIChomozygous128087958
4145340369145340369T13GENICpossibly homozygous132967616
4145337543145337544TC27GENIChomozygous119442637
4145339352145339353TC21GENIChomozygous112870782
4145339520145339521TG15GENIChomozygous119315383
4145339939145339940AG23GENIChomozygous119315384