chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184660235646602357AG24GENIChomozygous140307975
184660441846604419TC24GENIChomozygous140307976
184660550346605504GA20GENIChomozygous140307977
184660557146605572GA22GENIChomozygous140307978
184660746046607461AG12GENIChomozygous140307979
184660848246608483GA19GENIChomozygous140307980
184660947046609471GA22GENIChomozygous140307981
184660982446609825CT18GENIChomozygous140307982
184661119746611198GC13GENIChomozygous140307983
184661120746611208CT15GENIChomozygous140307984
184661182946611830CT23GENIChomozygous140307985
184661345146613452GT28GENIChomozygous140307986
184661389546613896AT26GENIChomozygous140307987
184661408846614089TC17GENIChomozygous140307988
184661411446614115CT18GENIChomozygous155089366
184661418746614188AG21GENIChomozygous140307989
184661443646614437AG17GENIChomozygous140307990
184661662446616625GA17GENIChomozygous140307991
184661411446614115C18GENICheterozygous403433348
184661411446614115CA18GENICheterozygous403433349
184661904546619049TTTG17GENIChomozygous140221372
184660790946607909TTTTTGA17GENIChomozygous140221368
184661713946617141CT17GENIChomozygous140221371
184661217546612175G23GENIChomozygous140221369
184662008246620083GA19GENIChomozygous140307992
184662082946620830A14GENIChomozygous403433350
184662082946620830AC14GENICheterozygous403433351
184662241446622415AT14GENIChomozygous140307993
184662371546623716AG20GENIChomozygous140307994
184662424646624246A17GENIChomozygous140221373
184662661646626617CG20GENIChomozygous140307995
184662705546627056CT17GENIChomozygous140307996
184662714746627148AG19GENIChomozygous140307997
184662894846628949CG15GENIChomozygous140307998
184663210646632107T20GENIChomozygous140221374
184663339646633396ACTTAAATTGATAATTTACAATAATGTACA9GENIChomozygous140221375
184663517846635178GTCTTGTCTT5GENICheterozygous140221376
184663518946635189TCTTGTCTTGTCTTTTCTTTTCTTTTCTTT5GENICheterozygous140221377
184663810946638110TC14GENIChomozygous140308000
184663973746639738AG18GENIChomozygous140308001