chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1178527033178527034AG36GENIChomozygous992686513
1178527146178527147AG25GENIChomozygous992686514
1178527407178527408CT35GENICpossibly homozygous992686515
1178527491178527492CT27GENICpossibly homozygous992686516
1178527527178527528CT27GENIChomozygous992686517
1178527838178527839AC19GENIChomozygous992686518
1178527840178527841TC19GENIChomozygous992686519
1178527932178527933TC23GENICpossibly homozygous992686520
1178528043178528044TA25GENIChomozygous992686521
1178528053178528054TC24GENIChomozygous992686522
1178528362178528363AG34GENICpossibly homozygous992686523
1178528372178528373GA33GENICpossibly homozygous992686524
1178528382178528383AG32GENICpossibly homozygous992686525
1178528591178528592CT23GENIChomozygous992686526
1178528663178528664CG23GENIChomozygous992686527
1178528698178528699TA22GENIChomozygous992686528
1178528746178528747TC19GENIChomozygous992686529
1178528787178528788TC17GENIChomozygous992686530
1178528963178528964AG23GENIChomozygous992686531
1178528991178528992TC21GENIChomozygous992686532
1178528993178528994GC21GENIChomozygous992686533
1178529004178529005GA20GENICpossibly homozygous992686534
1178529018178529019TC26GENICpossibly homozygous992686535
1178530290178530291AG16GENICpossibly homozygous992686536
1178530738178530739CA27GENIChomozygous992686537
1178531549178531550TC19GENIChomozygous992686538
1178531581178531582CT22GENIChomozygous992686539
1178531623178531624TG26GENIChomozygous992686540
1178531930178531931TC26GENIChomozygous992686541
1178533353178533354TC34GENICpossibly homozygous992686542
1178533797178533798AG18GENIChomozygous992686543
1178534097178534098AG17GENIChomozygous992686544
1178534954178534955CG18GENICpossibly homozygous992686545