chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115340075115340076GT19GENIChomozygous126022321
4115343513115343514AG12GENICheterozygous126118280
4115352852115352853TC11GENIChomozygous126022322
4115352863115352864TG11GENIChomozygous126022323
4115352890115352891TA7GENIChomozygous126022324
4115354428115354429TC14GENIChomozygous126022325
4115354429115354430AC12GENIChomozygous126022326
4115354900115354901AC16GENIChomozygous126022327
4115354928115354929GA7GENIChomozygous126022328
4115354932115354933GT8GENIChomozygous126022329
4115354937115354938TA5GENIChomozygous126022330
4115354938115354939TC7GENIChomozygous126022331
4115353304115353305GA4GENIChomozygous126149270