chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2142482409142482410G-10GENICheterozygous59870354
2142482816142482817AC13GENIChomozygous59130298
2142482888142482889CT14GENIChomozygous59870355
2142483162142483163TC24GENIChomozygous59130300
2142485687142485688GGTGGAGGAGCATGC23GENIChomozygous59130310
2142485963142485964A-24GENIChomozygous59130312
2142487041142487042TTTTGA20GENIChomozygous59870356
2142487131142487132CA33GENIChomozygous59130315
2142487539142487540CCAACTCTCAGTTCCTTTCTCCCG23GENIChomozygous60500372
2142487741142487742AT17GENIChomozygous59130320
2142488627142488628GT17GENIChomozygous59130322
2142488738142488739AG21GENIChomozygous59870357
2142488780142488781GA15GENIChomozygous59130324
2142489078142489079GGAAA7GENICpossibly homozygous60216055
2142489749142489750TC20GENIChomozygous59870359
2142490080142490081C-30GENIChomozygous59130328
2142490293142490294CT25GENIChomozygous59870360
2142491308142491309CT29GENIChomozygous59870361
2142492423142492424T-7GENIChomozygous59870362
2142492568142492569TTTTTTC7GENICheterozygous59870363
2142495236142495237GA29GENIChomozygous59870367
2142495992142495993A-11GENIChomozygous59761173
2142496006142496007A-14GENIChomozygous59870368
2142496158142496159TTGG5GENIChomozygous59870369
2142497646142497647AT30GENIChomozygous59870370
2142497727142497728CT23GENIChomozygous59870371