chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205047215205047216GT9GENIChomozygous61063956
1205047451205047452AAG14GENIChomozygous61063957
1205048085205048086CCTT8GENIChomozygous61585399
1205049318205049319CCTT8GENICheterozygous61063959
1205050460205050461T-17GENIChomozygous61063964
1205050460205050461TTG17GENIChomozygous61063965
1205050490205050491A-8GENIChomozygous61063966
1205052758205052759AG22GENIChomozygous61063971
1205055146205055148TT--8GENICheterozygous61585400
1205055147205055148T-8GENICheterozygous61682505
1205056604205056605AAG7GENICheterozygous61063973
1205057339205057340CA15GENICheterozygous61063975
1205057600205057602AA--4GENIChomozygous61063977
1205057869205057870T-11GENICheterozygous61063979
1205057931205057932AAT14GENICpossibly homozygous61063980
1205059748205059749AG32GENIChomozygous61063985
1205060163205060164TC19GENIChomozygous61063989
1205060169205060170AC19GENIChomozygous61063990
1205062431205062432GGA19GENICpossibly homozygous61585401
1205063150205063151TG29GENIChomozygous61063993
1205066432205066433GGCA6GENICheterozygous61318261
1205066748205066749T-5GENICheterozygous61585402
1205067677205067691TTTTTTTTTTTTTT--------------6GENIChomozygous61585403
1205070052205070053AG21GENICheterozygous61585404
1205070415205070416AG28GENIChomozygous61064003
1205072732205072733CCTT5GENIChomozygous61585405
1205073081205073082TTGACAGGCGAGTGG33GENIChomozygous61064007
1205076510205076511A-2GENICheterozygous61064013