chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2142482409142482410G-1GENIChomozygous59870354
2142482420142482421T-16GENICheterozygous59130292
2142482816142482817AC20GENIChomozygous59130298
2142482888142482889CT26GENICpossibly homozygous59870355
2142483162142483163TC33GENIChomozygous59130300
2142485687142485688GGTGGAGGAGCATGC16GENIChomozygous59130310
2142485963142485964A-15GENIChomozygous59130312
2142487041142487042TTTTGA25GENIChomozygous59870356
2142487131142487132CA22GENIChomozygous59130315
2142487741142487742AT18GENIChomozygous59130320
2142488627142488628GT34GENIChomozygous59130322
2142488738142488739AG54GENIChomozygous59870357
2142488780142488781GA43GENIChomozygous59130324
2142489078142489079GGAAA3GENIChomozygous60216055
2142489749142489750TC32GENIChomozygous59870359
2142490080142490081C-21GENIChomozygous59130328
2142490293142490294CT14GENIChomozygous59870360
2142491308142491309CT34GENICpossibly homozygous59870361
2142492423142492424T-10GENIChomozygous59870362
2142492568142492569TTTTTTC11GENIChomozygous59870363
2142493150142493151TC10GENIChomozygous59870364
2142493261142493262AT13GENIChomozygous59870365
2142493333142493334GA9GENIChomozygous59870366
2142495236142495237GA24GENIChomozygous59870367
2142495992142495993A-1GENIChomozygous59761173
2142496006142496007A-22GENICpossibly homozygous59870368
2142496158142496159TTGG15GENIChomozygous59870369
2142497646142497647AT27GENIChomozygous59870370
2142497727142497728CT28GENIChomozygous59870371