chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
329087552908756AG16GENIChomozygous111429617
329088002908801CT14GENIChomozygous111429618
329088462908847CT14GENIChomozygous111429619
329089832908984CG18GENIChomozygous111429620
329091862909187GT8GENIChomozygous111429621
329092072909208TA8GENIChomozygous111429622
329093752909376AC10GENIChomozygous111429623
329093882909389AT10GENIChomozygous111429624
329094192909420AC7GENIChomozygous127966408
329094202909421GA7GENIChomozygous127966409
329094262909427AC8GENIChomozygous127966410
329094272909428GA8GENIChomozygous127966411
329094302909431GA8GENIChomozygous111429625
329095602909561TC33GENICheterozygous111429626
329095852909586TC29GENICheterozygous111429627
329096092909610GT27GENICheterozygous111429628
329096452909646TA20GENIChomozygous111429629
329098742909875AG8GENIChomozygous127966412
329099532909954TG11GENIChomozygous111429630
329106732910674GA11GENIChomozygous111429631
329107542910755TC18GENIChomozygous111429632
329108982910899GT13GENIChomozygous111429633
329109022910903TA13GENIChomozygous111429634
329111582911159CA20GENIChomozygous111429635
329111732911174CT18GENIChomozygous111429636
329112112911212CT16GENIChomozygous111429637
329114082911409CT13GENIChomozygous111429638
329114742911475TC17GENIChomozygous111429639
329117152911716CT16GENIChomozygous111429640
329128132912814TC10GENIChomozygous111429641
329128222912823TC10GENIChomozygous111429642
329128532912854CT16GENIChomozygous111429643
329129122912913CT21GENIChomozygous111429644
329129522912953CG21GENIChomozygous111429645
329120922912093CT16GENIChomozygous119960827