chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71458917714589178CCA7GENIChomozygous53798396
71459057514590579TATC----5GENIChomozygous53798405
71459208714592089TG--11GENICheterozygous55071997
71459527314595277CTTC----6GENIChomozygous55071999
71459746414597466TG--11GENICheterozygous55021252
71459829314598294A-15GENIChomozygous53798429
71459937014599371G-13GENICheterozygous55021253
71459937214599373AAG13GENICheterozygous54955984
71460021614600217T-5GENICheterozygous53798443
71459070214590703TTTCTA2GENIChomozygous54303345
71460079614600800GTCA----8GENIChomozygous54303348
71460794714607948AAGTGT5GENICheterozygous54956008
71460870314608705GT--24GENICheterozygous55072003
71461970714619708TTA19GENICheterozygous54182178
71462529514625296C-10GENICpossibly homozygous55072005
71463238214632384TG--13GENICheterozygous53798612
71465370414653705CCAGAGAG6GENICheterozygous54956053
71465370414653705CCAGAGAGAG6GENICheterozygous55021257
71465719714657201AAAG----10GENIChomozygous54303358
71466075214660753GGA15GENICheterozygous53798772
71466246814662472GTGT----9GENICheterozygous55072011
71466247014662472GT--9GENICheterozygous55072013
71466548014665481AACTGAGG27GENIChomozygous53798811
71466761114667612T-16GENICheterozygous55172228
71460794714607948AAGT5GENICheterozygous55845944
71461478114614782GGCTCT5GENIChomozygous55845947