chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205047215205047216GT20GENIChomozygous61063956
1205047451205047452AAG24GENIChomozygous61063957
1205048085205048086CCT22GENICpossibly homozygous61585398
1205048085205048086CCTT22GENICheterozygous61585399
1205050460205050461TTG27GENIChomozygous61063965
1205050495205050496GGTGTGTGTGTGTGTGTGT8GENIChomozygous62236100
1205051359205051360AATGTG4GENICheterozygous62413307
1205057339205057340CA9GENIChomozygous61063975
1205057360205057361CA12GENICpossibly homozygous62095802
1205057600205057602AA--23GENICheterozygous61063977
1205057601205057602A-23GENICheterozygous61063978
1205057845205057846T-16GENICheterozygous62248591
1205058103205058104GGT16GENICheterozygous62248592
1205058104205058105T-16GENICheterozygous61063981
1205059748205059749AG10GENIChomozygous61063985
1205060163205060164TC13GENIChomozygous61063989
1205060169205060170AC13GENIChomozygous61063990
1205060408205060409TTTG2GENIChomozygous62192389
1205060411205060412CCTTG2GENIChomozygous62192391
1205060412205060413CCTAGG2GENIChomozygous62192393
1205060420205060424CGTG----5GENIChomozygous62192395
1205060426205060427TTCTACCAC6GENIChomozygous62192397
1205060429205060430AAGCTAAATCC7GENIChomozygous62192398
1205061390205061391CCA16GENICheterozygous62236102
1205062256205062257C-5GENICheterozygous62248593
1205066432205066433GGCA5GENICheterozygous61318261
1205066762205066763G-22GENICheterozygous62236104
1205070008205070009AATGTGTGTGTGTG8GENICheterozygous62236106
1205070008205070009AATGTGTGTGTGTGTGTG8GENICpossibly homozygous62192402
1205073360205073361CCGT7GENICheterozygous62192404
1205073360205073361CCGTGT7GENICheterozygous62192406
1205076510205076511A-10GENICheterozygous61064013
1205078076205078077TC33GENIChomozygous62030221