chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3151232967151232968TC31GENIChomozygous111776592
3151234493151234494CT15GENIChomozygous111776596
3151234781151234782AG60GENIChomozygous111776598
3151234912151234913TC30GENIChomozygous112431627
3151235365151235366AG34GENICpossibly homozygous111776600
3151235791151235792GC65GENIChomozygous112431628
3151237769151237770CT31GENIChomozygous112431629
3151239526151239527CA23GENIChomozygous112431630
3151240570151240571CT16GENIChomozygous112041535
3151242187151242188GA32GENIChomozygous112431631
3151248171151248172CT37GENIChomozygous112041539
3151248227151248228TG53GENIChomozygous112431632
3151250680151250681AG18GENIChomozygous111776612
3151251100151251101TG55GENIChomozygous112431633
3151251428151251429AT28GENIChomozygous112431634
3151251550151251551CA17GENIChomozygous112431635
3151252140151252141CT51GENIChomozygous112431636
3151252215151252216CA40GENIChomozygous111776616
3151252795151252796CG51GENIChomozygous112431637
3151256132151256133AG46GENIChomozygous112431638
3151256328151256329GT11GENICpossibly homozygous112431639