chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1143096388143096389GA15GENICpossibly homozygous60877287
1143096837143096838TTTTTTTGTTTTTG1GENIChomozygous60877288
1143097240143097241GA10GENIChomozygous60877289
1143098372143098373AAC19GENICheterozygous60877291
1143101883143101884GA19GENIChomozygous60877293
1143102879143102880AT6GENICheterozygous62089381
1143102987143102988AG21GENIChomozygous60877295
1143104430143104431TC15GENIChomozygous60877296
1143104527143104528GT12GENIChomozygous60877297
1143106171143106172TC15GENICheterozygous60877306
1143107438143107439CA32GENICpossibly homozygous60877307
1143107935143107936TG24GENICpossibly homozygous60877308
1143108004143108005TC18GENICpossibly homozygous60877309
1143109250143109251CT20GENICpossibly homozygous60877311
1143109927143109928TA25GENICpossibly homozygous60877312
1143110397143110409CACACATATACG------------1GENIChomozygous60877315
1143110687143110688TTA15GENICpossibly homozygous60877317
1143111537143111538TC17GENIChomozygous62089382
1143111849143111850GA16GENICpossibly homozygous60877323
1143112773143112774AG13GENICpossibly homozygous60877324
1143113079143113080TC26GENICpossibly homozygous60877325
1143113449143113450TC17GENIChomozygous60877326
1143113795143113796TC15GENIChomozygous60877327
1143115332143115333GA12GENICheterozygous60877332
1143115869143115870CA25GENICpossibly homozygous60877333
1143116009143116010GA27GENIChomozygous60877334
1143116170143116171TC3GENIChomozygous60877335
1143116379143116380TC11GENICpossibly homozygous60877336
1143116387143116388C-7GENICheterozygous60877338
1143116474143116475GA14GENIChomozygous60877340