chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2225335880225335881AG27GENIChomozygous110271374
2225335973225335974AC30GENIChomozygous110271376
2225336016225336017AG30GENIChomozygous110271378
2225336030225336031AT32GENIChomozygous110271380
2225336115225336116GA50GENIChomozygous110271382
2225336376225336377GC35GENIChomozygous110271384
2225339986225339987GA25GENIChomozygous110271386
2225341006225341007CT35GENIChomozygous110271388
2225341839225341840CT18GENIChomozygous110271390
2225342279225342280AT20GENIChomozygous110271392
2225342688225342689CT36GENIChomozygous110271394
2225342872225342873TC34GENIChomozygous110271396
2225343337225343338AG41GENIChomozygous110271398
2225343540225343541TA31GENIChomozygous110271400
2225343762225343763AG22GENIChomozygous110271402
2225349159225349160AG25GENIChomozygous110271404
2225350344225350345GA28GENIChomozygous110271406
2225350379225350380GA29GENIChomozygous110271408
2225353422225353423TG33GENIChomozygous110271410
2225354551225354552GA19GENIChomozygous110271412
2225357857225357858AG32GENIChomozygous110271414
2225358276225358277AG15GENIChomozygous110271416
2225358642225358643AG44GENICpossibly homozygous110271418
2225359573225359574AG11GENIChomozygous110271420
2225359597225359598CA11GENICpossibly homozygous110271422
2225363617225363618AT44GENIChomozygous110271424
2225366126225366127GA19GENIChomozygous110271428
2225367436225367437GA22GENIChomozygous110271430
2225367686225367687AG31GENIChomozygous110271432
2225368407225368408TG30GENIChomozygous110271434
2225379853225379854TG6GENIChomozygous110271440
2225369988225369989GA31GENIChomozygous110271436
2225371001225371002AG15GENIChomozygous110271438