chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2142481904142481910ACACAC------1GENIChomozygous60500371
2142482409142482410G-4GENIChomozygous59870354
2142482816142482817AC16GENIChomozygous59130298
2142482888142482889CT18GENIChomozygous59870355
2142483162142483163TC15GENIChomozygous59130300
2142485687142485688GGTGGAGGAGCATGC29GENIChomozygous59130310
2142485963142485964A-25GENIChomozygous59130312
2142487041142487042TTTTGA21GENIChomozygous59870356
2142487131142487132CA20GENIChomozygous59130315
2142487539142487540CCAACTCTCAGTTCCTTTCTCCCG27GENIChomozygous60500372
2142487741142487742AT25GENIChomozygous59130320
2142488627142488628GT7GENIChomozygous59130322
2142488738142488739AG6GENIChomozygous59870357
2142488780142488781GA12GENIChomozygous59130324
2142489078142489079GGAAA5GENIChomozygous60216055
2142489749142489750TC10GENIChomozygous59870359
2142490080142490081C-15GENIChomozygous59130328
2142490293142490294CT29GENIChomozygous59870360
2142491308142491309CT23GENIChomozygous59870361
2142492423142492424T-10GENIChomozygous59870362
2142492568142492569TTTTTTC5GENICheterozygous59870363
2142495236142495237GA19GENIChomozygous59870367
2142496006142496007A-33GENICpossibly homozygous59870368
2142496158142496159TTGG11GENIChomozygous59870369
2142497646142497647AT29GENIChomozygous59870370
2142497727142497728CT37GENIChomozygous59870371
2142495992142495993A-29GENICpossibly homozygous59761173