chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102901649029016491GA39GENIChomozygous116750921
102901663229016633TA39GENICheterozygous118127973
102901663529016636AG38GENICheterozygous118127974
102901664929016650GC36GENICheterozygous118127975
102901665429016655GT35GENICheterozygous118127976
102901666229016663CT33GENICheterozygous118127977
102901731629017317AG20GENIChomozygous116538952
102901815229018153GA45GENIChomozygous116750923
102901914929019150AG43GENIChomozygous116538954
102902020729020208GA29GENIChomozygous117001324
102902030829020309CT5GENIChomozygous116538956
102902165929021660TC14GENIChomozygous116750925
102902192029021921GA36GENIChomozygous116538960
102902228429022285CA29GENIChomozygous116538962
102902228929022290GA32GENIChomozygous116538964
102902231429022315AC30GENIChomozygous116538966
102902252729022528AG24GENICpossibly homozygous118121517
102902368429023685GA24GENIChomozygous116750927
102902379329023794AG26GENIChomozygous116538970
102902392029023921CT39GENIChomozygous116538974
102902398329023984CT34GENIChomozygous116538976
102902398729023988CT34GENIChomozygous116538980
102902419229024193CT40GENIChomozygous116538988
102902441229024413TC25GENIChomozygous116750929
102902465629024657CA33GENIChomozygous116750931
102902488429024885GA32GENIChomozygous116538990
102902515529025156CG26GENIChomozygous116538992
102902521229025213TG31GENIChomozygous116750933