chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3161802581161802582CT11GENIChomozygous141561676
3161803824161803825AG18GENIChomozygous141561677
3161804293161804294TG16GENIChomozygous141561678
3161804587161804588AG6GENIChomozygous141561679
3161807037161807038GA19GENIChomozygous141561680
3161807646161807647TG13GENIChomozygous141561681
3161809345161809360GAGGGCCGTGATAAG9GENIChomozygous141485987
3161810058161810061GTG12GENIChomozygous141485988
3161810206161810206ACACACGT11GENIChomozygous141485989
3161810313161810314AG19GENIChomozygous141561682
3161810640161810641TC14GENIChomozygous141561683
3161810827161810828TG27GENIChomozygous141561684
3161813278161813279TC3GENIChomozygous141561685