chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184660235646602357AG47GENIChomozygous140307975
184660441846604419TC20GENIChomozygous140307976
184660550346605504GA21GENIChomozygous140307977
184660557146605572GA29GENIChomozygous140307978
184660746046607461AG36GENIChomozygous140307979
184660848246608483GA27GENIChomozygous140307980
184660947046609471GA34GENIChomozygous140307981
184660982446609825CT29GENIChomozygous140307982
184661119746611198GC16GENIChomozygous140307983
184661120746611208CT18GENIChomozygous140307984
184661182946611830CT23GENIChomozygous140307985
184661345146613452GT30GENIChomozygous140307986
184661389546613896AT38GENIChomozygous140307987
184661408846614089TC16GENICheterozygous140307988
184661411446614115CT13GENICheterozygous155089366
184661418746614188AG18GENIChomozygous140307989
184661443646614437AG27GENIChomozygous140307990
184661411446614115C13GENICheterozygous403433348
184661411446614115CA13GENICheterozygous403433349
184661662446616625GA23GENIChomozygous140307991
184661713946617141CT26GENIChomozygous140221371
184660790946607909TTTTTGA26GENIChomozygous140221368
184661217546612175G31GENIChomozygous140221369
184661409346614099ATATAC16GENICheterozygous140221370
184661904546619049TTTG20GENIChomozygous140221372
184662008246620083GA27GENIChomozygous140307992
184662082946620830A18GENICheterozygous403433350
184662082946620830AC18GENICheterozygous403433351
184662241446622415AT29GENIChomozygous140307993
184662371546623716AG16GENIChomozygous140307994
184662424646624246A29GENIChomozygous140221373
184662661646626617CG18GENIChomozygous140307995
184662705546627056CT24GENIChomozygous140307996
184662714746627148AG32GENIChomozygous140307997
184662894846628949CG30GENIChomozygous140307998
184663210646632107T33GENIChomozygous140221374
184663339646633396ACTTAAATTGATAATTTACAATAATGTACA13GENIChomozygous140221375
184663810946638110TC26GENIChomozygous140308000
184663973746639738AG27GENIChomozygous140308001
184662828546628286CT30GENIChomozygous148131463