chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13110741872110741873TC19GENIChomozygous942065117
13110742696110742697AG27GENIChomozygous942065118
13110743778110743779CT26GENIChomozygous942065119
13110743788110743789CT30GENIChomozygous942065120
13110743858110743859GA37GENIChomozygous942065121
13110743981110743982TC35GENIChomozygous942065122
13110744513110744514AG32GENIChomozygous942065123
13110744526110744527CT34GENIChomozygous942065124
13110745556110745557AG34GENIChomozygous942065125
13110745588110745589AG34GENIChomozygous942065126
13110746430110746431CT22GENIChomozygous942065127
13110746508110746509CT23GENIChomozygous942065128
13110746797110746798CT25GENIChomozygous942065129
13110747171110747172TC38GENIChomozygous942065130
13110748032110748033AC33GENIChomozygous942065131
13110748585110748586CT35GENIChomozygous942065132
13110748713110748714TC30GENIChomozygous942065133
13110748723110748724TC33GENIChomozygous942065134
13110748906110748907AG33GENIChomozygous942065135