chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
329087552908756AG47GENIChomozygous111429617
329088002908801CT60GENIChomozygous111429618
329088462908847CT61GENIChomozygous111429619
329089832908984CG70GENIChomozygous111429620
329091862909187GT43GENIChomozygous111429621
329092072909208TA47GENIChomozygous111429622
329093752909376AC28GENIChomozygous111429623
329093882909389AT27GENIChomozygous111429624
329094192909420AC23GENIChomozygous127966408
329094202909421GA22GENIChomozygous127966409
329094262909427AC21GENIChomozygous127966410
329094272909428GA23GENIChomozygous127966411
329094302909431GA23GENIChomozygous111429625
329095562909559CCC71GENICheterozygous129887322
329095602909561TC81GENICheterozygous111429626
329095602909560GTC71GENICheterozygous129887323
329095852909586TC79GENICheterozygous111429627
329096092909610GT70GENICheterozygous111429628
329096452909646TA53GENIChomozygous111429629
329098742909875AG17GENIChomozygous127966412
329099532909954TG34GENIChomozygous111429630
329106732910674GA56GENIChomozygous111429631
329107542910755TC54GENIChomozygous111429632
329108982910899GT60GENIChomozygous111429633
329109022910903TA60GENIChomozygous111429634
329111582911159CA54GENIChomozygous111429635
329111732911174CT53GENIChomozygous111429636
329112112911212CT58GENIChomozygous111429637
329114082911409CT54GENIChomozygous111429638
329114742911475TC61GENIChomozygous111429639
329117152911716CT55GENIChomozygous111429640
329128132912814TC53GENIChomozygous111429641
329128222912823TC59GENIChomozygous111429642
329128532912854CT64GENIChomozygous111429643
329120922912093CT64GENIChomozygous119960827
329129122912913CT66GENIChomozygous111429644
329129522912953CG71GENIChomozygous111429645