chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5157802718157802718GC17GENIChomozygous128263017
5157802719157802720TC18GENIChomozygous114070479
5157802729157802729G18GENIChomozygous128263018
5157802733157802733C18GENIChomozygous128263019
5157802734157802735TA18GENIChomozygous122426933
5157802742157802742C18GENIChomozygous128263020
5157802752157802752C19GENIChomozygous128263021
5157802761157802761T16GENIChomozygous128263022
5157802779157802779C14GENIChomozygous128263023
5157802785157802785C13GENIChomozygous128263024
5157802807157802808T10GENIChomozygous128263025
5157802819157802819A7GENIChomozygous128263026
5157802821157802821T6GENIChomozygous128263027
5157802826157802826C6GENIChomozygous128263028
5157802831157802831CA5GENIChomozygous128263029
5157802838157802839GT5GENIChomozygous122426944
5157802840157802841T5GENIChomozygous128263030
5157802853157802853C4GENIChomozygous128263031
5157807995157808002CTAGGGG5GENIChomozygous128263032
5157808576157808577TA12GENIChomozygous114070480
5157809729157809730TC7GENIChomozygous114070481
5157810319157810320AG10GENIChomozygous114070482
5157810870157810871AG21GENIChomozygous114070483
5157812510157812510G17GENIChomozygous128263033
5157812511157812514GAA17GENIChomozygous128263034
5157812766157812766A22GENIChomozygous128263035