chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X8606850486068505GT12GENICpossibly homozygous45161979
X8607867686078677G-4GENIChomozygous45161994
X8608468486084685TC3GENICheterozygous45161997
X8609176586091766CCA12GENIChomozygous45162001
X8611288186112883TT--1GENIChomozygous45162025
X8611292186112922GGA1GENIChomozygous45162027
X8611293886112939T-3GENIChomozygous45162028
X8611294886112949TTTA4GENIChomozygous45162029
X8611298086112981AAT5GENIChomozygous45479685
X8611298486112985TTA6GENIChomozygous45162030
X8611302986113030GT5GENICheterozygous45261970
X8611303586113036C-3GENICheterozygous45162031
X8611303886113039CA2GENIChomozygous45515991
X8611304586113046C-2GENIChomozygous45261971
X8611306586113066GT5GENIChomozygous45162032
X8611307286113073GT7GENIChomozygous45162033
X8611796486117965TC4GENICheterozygous45162037
X8612795686127957TG3GENICheterozygous45162054
X8613166286131663AACT3GENICheterozygous45732637
X8613166486131666CA--3GENICheterozygous45732639
X8613459686134597CG4GENIChomozygous45162078
X8613734986137350TA6GENICheterozygous45162083
X8614773186147732TC10GENICheterozygous45349540