chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135963357135963358GA27GENIChomozygous114018739
5135963921135963922AG26GENIChomozygous114018740
5135964264135964265AG25GENIChomozygous114018741
5135964835135964836GA17GENIChomozygous114018742
5135965311135965312AG27GENIChomozygous114018743
5135965675135965676GT20GENIChomozygous114018744
5135966183135966184AT25GENIChomozygous114018745
5135967576135967577CT19GENIChomozygous114018746
5135968347135968348TC26GENIChomozygous114018747
5135968788135968789CT22GENIChomozygous114018748
5135969112135969113AG29GENIChomozygous114018749
5135969913135969914TC17GENIChomozygous114018750
5135970528135970529AT25GENIChomozygous114018751
5135970722135970723GT21GENIChomozygous114018752
5135972981135972982GT36GENIChomozygous114018753
5135973426135973427GA31GENIChomozygous114018754
5135974978135974979AG31GENIChomozygous114018755
5135977808135977809CT40GENIChomozygous114018756
5135977966135977967GA35GENIChomozygous114018757
5135978092135978093CT32GENIChomozygous114018758
5135980630135980631CT26GENIChomozygous114018759
5135980996135980997AG30GENIChomozygous114018760
5135982185135982186GA29GENIChomozygous114018761
5135982627135982628AG31GENIChomozygous114018762
5135982678135982679AG29GENIChomozygous114018763
5135982688135982689AT29GENIChomozygous114018764