chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2180898138180898139AG12GENIChomozygous957366249
2180898172180898173GA21GENIChomozygous957366250
2180899134180899135GA18GENIChomozygous957366251
2180899312180899313AG16GENIChomozygous957366252
2180899631180899632TC16GENIChomozygous957366253
2180899755180899756CT11GENIChomozygous957366254
2180901332180901333TC24GENIChomozygous957366255
2180902408180902409AG18GENIChomozygous957366256
2180903152180903153AT8GENIChomozygous957366257
2180906629180906630AC14GENIChomozygous957366258
2180907151180907152TC9GENIChomozygous957366259
2180907719180907720TA12GENIChomozygous957366260
2180908056180908057TA22GENIChomozygous957366261
2180908111180908112GA18GENIChomozygous957366262
2180910701180910702AC17GENIChomozygous957366263
2180911479180911480TC24GENIChomozygous957366264
2180911824180911825CG22GENIChomozygous957366265
2180911828180911829GA22GENIChomozygous957366266