chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3147827893147827894GA18GENIChomozygous60273985
3147829890147829891G-13GENICpossibly homozygous59238432
3147830340147830343CCC---17GENIChomozygous57728485
3147830381147830382AG19GENIChomozygous58225116
3147830481147830482GA13GENIChomozygous60286223
3147830744147830745TC19GENIChomozygous60273986
3147831074147831075AG18GENICheterozygous58225117
3147831082147831083TC20GENICheterozygous58225118
3147831207147831208GT18GENIChomozygous57728489
3147832764147832765AT13GENIChomozygous57728491
3147833214147833215GC25GENIChomozygous57728493
3147833247147833248TC24GENICpossibly homozygous57728495
3147834054147834055AC22GENIChomozygous57728501
3147834122147834123C-19GENIChomozygous58225120
3147834195147834196AT21GENICpossibly homozygous58753031
3147834975147834976TTAA17GENICheterozygous57728503
3147834975147834976TTA17GENICheterozygous58753033
3147835175147835176GA20GENICpossibly homozygous60273987
3147835412147835413CCCTTCCTTT17GENICpossibly homozygous60273988
3147836004147836005AG20GENIChomozygous58225122
3147836531147836533CC--12GENIChomozygous58753035
3147836695147836696CA23GENIChomozygous60273989
3147837511147837512GA12GENICpossibly homozygous60273990
3147837882147837883TC18GENIChomozygous60286225