chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104497795544977956GT17GENIChomozygous51441478
104497798944977990CT15GENIChomozygous52244805
104497805444978055TG18GENIChomozygous52192851
104497819144978192CT20GENIChomozygous51441480
104497828344978284A-14GENIChomozygous51441482
104497850544978506CA18GENIChomozygous51441483
104497906844979070AA--9GENIChomozygous51441484
104497913244979133GC4GENIChomozygous51441485
104498190144981902TC31GENIChomozygous52317893
104498343644983437GA23GENIChomozygous51441487
104498366744983675AAAGAACA--------11GENICheterozygous51441488
104498367144983675AACA----11GENICheterozygous51441489
104498399644984006ACACACACAC----------17GENICheterozygous52372805
104498399844984006ACACACAC--------17GENICpossibly homozygous52372807
104498600744986008CCA17GENICheterozygous52438974
104498686544986867TG--3GENIChomozygous52647962
104498686644986867GGCCC3GENIChomozygous52647966
104499122244991223CT33GENIChomozygous51441533
104499163844991639CT15GENIChomozygous51441534
104499192944991930C-11GENIChomozygous51441535
104499233544992336TC20GENIChomozygous51441536
104499289144992892CCAAA7GENICheterozygous51441537
104499337144993372AAGAG29GENIChomozygous51441539
104499448344994487GCAC----29GENIChomozygous51441540
104499566244995664AT--3GENIChomozygous51441541
104499567044995672AA--3GENIChomozygous51441543
104499569444995697AAA---3GENIChomozygous51441544
104499570144995706TAAAT-----2GENIChomozygous51441545
104499646144996465CATA----19GENIChomozygous51441546
104499650844996509CCCTGT30GENIChomozygous51441548
104499717044997178CGCGCACA--------18GENICpossibly homozygous51441549
104499762244997623AG17GENIChomozygous51441550
104499776544997766TC21GENIChomozygous51441551
104499818744998188TTAA7GENIChomozygous51635832
104499918144999182TC19GENIChomozygous51441553
104499986144999862TC39GENIChomozygous51441554