chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8111248726111248727AAAAAGG17GENIChomozygous52806297
8111249550111249551AG12GENIChomozygous52806303
8111249717111249721TATT----6GENIChomozygous53522720
8111249980111249981CCA18GENIChomozygous52806309
8111250316111250317AG30GENIChomozygous52806321
8111250038111250039AG21GENIChomozygous52806312
8111250068111250069AG17GENIChomozygous52806315
8111250231111250232CT27GENIChomozygous52806318
8111250465111250466CCA39GENIChomozygous52806324
8111250472111250473CA40GENIChomozygous52806327
8111251034111251035CT31GENIChomozygous52806337
8111250481111250482GT37GENIChomozygous52806329
8111250541111250542AC23GENIChomozygous52806332
8111250973111250974AG22GENIChomozygous52806334
8111251156111251157TA33GENIChomozygous52806340
8111251320111251321AC28GENIChomozygous52806343
8111251430111251431GC34GENIChomozygous52806346
8111251439111251440CT34GENIChomozygous52806349
8111251607111251608CT29GENIChomozygous52806352
8111251891111251892AT40GENIChomozygous52806355
8111252043111252044TC38GENIChomozygous52806358
8111252101111252102AC30GENIChomozygous52806361
8111252158111252159TC33GENIChomozygous52806364
8111252428111252429GA38GENIChomozygous52806367
8111253132111253133GGGCT30GENIChomozygous52806370
8111253681111253682GA35GENIChomozygous52806372
8111253974111253975GT28GENIChomozygous52806375
8111254517111254518CT36GENIChomozygous52806378
8111255083111255084AG23GENIChomozygous52806381
8111255426111255427AT28GENIChomozygous52806383