chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2250997221250997222GT20GENIChomozygous110382243
2250998053250998054AG24GENIChomozygous110382245
2250998627250998628CT19GENIChomozygous111035748
2250998847250998848CT14GENIChomozygous110382251
2250999575250999576CA20GENIChomozygous111035750
2251000529251000530GA19GENIChomozygous110382253
2251000718251000719AT22GENIChomozygous110382254
2251000803251000804CT7GENIChomozygous110852151
2251000849251000850AC10GENIChomozygous110852153
2251000926251000927GA12GENIChomozygous110852155
2251002391251002392CT23GENIChomozygous111035754
2251003077251003078GT16GENIChomozygous111035756
2251004184251004185TG4GENIChomozygous125751488
2251009440251009441AG21GENIChomozygous110382286
2251010573251010574TG22GENIChomozygous110852179
2251012813251012814CA20GENIChomozygous111035762
2251012927251012928GA29GENIChomozygous111035764
2251014545251014546CA4GENIChomozygous111035770
2251016964251016965AG17GENIChomozygous110382322
2251018523251018524TG17GENIChomozygous110382328
2251020803251020804TA15GENIChomozygous110852204
2251021160251021161CT6GENIChomozygous111035786
2251021161251021162AG6GENIChomozygous110382332
2251021166251021167AG10GENIChomozygous110382334
2251021715251021716GA21GENIChomozygous111035788
2251022350251022351TC18GENIChomozygous110382336
2251023206251023207AG15GENIChomozygous110382338
2251024130251024131AG27GENIChomozygous110382340
2251029266251029267AG19GENIChomozygous110382354
2251030849251030850AG7GENIChomozygous110382360