chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
385353768535377CT17GENIChomozygous111441878
385376008537601TC27GENIChomozygous111441879
385387338538734TC26GENIChomozygous111441880
385406718540672TC16GENIChomozygous111441881
385422098542210CT18GENIChomozygous111441882
385425358542536CT16GENIChomozygous111441883
385428638542864TC15GENIChomozygous125806761
385453318545332GA20GENICpossibly homozygous111441884
385472188547219AG23GENIChomozygous111441885
385504058550406AG13GENIChomozygous112222915
385543758554376AG15GENIChomozygous111441886
385592188559219GC25GENIChomozygous111441887
385594948559495GA12GENIChomozygous111441888
385601508560151TC15GENIChomozygous112222921
385601518560152AT15GENIChomozygous111441890
385608688560869AG23GENIChomozygous111441891
385614398561440AG32GENIChomozygous111441892
385633428563342G3GENIChomozygous127847938
385485178548517A16GENIChomozygous127847935
385506908550690T24GENICpossibly homozygous127847936
385597108559711A6GENIChomozygous127847937
385504068550407GC13GENIChomozygous119647576
385597128559713AG6GENIChomozygous127968178
385649678564968AC11GENIChomozygous111441893
385656828565683TC11GENIChomozygous111441894
385692438569244CG29GENIChomozygous111441895
385709608570961TG15GENIChomozygous111441896
385731098573110CG10GENIChomozygous111441897
385752678575268TC15GENIChomozygous111441898
385785278578528GT20GENIChomozygous111441900
385787918578792TC14GENIChomozygous111441901
385790108579011CT26GENICpossibly homozygous111441902
385801558580156GA22GENIChomozygous111441903
385809998581000AT10GENICpossibly homozygous111441904
385812668581267CA10GENIChomozygous111441905
385859498585950AG21GENIChomozygous111441906
385878088587809GA22GENICpossibly homozygous111441907
385902508590251AG18GENIChomozygous111441908
385903388590339CT14GENIChomozygous111441909
385904308590431GC16GENIChomozygous111441910
385964668596466C20GENIChomozygous127847939
385970348597035TC23GENIChomozygous111441911
385988998598900CT21GENIChomozygous111441912