chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1190498476190498477GA13GENIChomozygous141289583
1190498505190498506CT17GENIChomozygous141289584
1190498586190498587AG27GENIChomozygous141289585
1190498607190498608GA27GENIChomozygous141289586
1190502192190502193GA21GENIChomozygous141289587
1190502427190502428GA14GENIChomozygous141289588
1190505866190505867AG10GENICheterozygous404610503
1190505894190505895TC10GENIChomozygous141289589
1190506314190506315GA12GENIChomozygous141289590
1190506697190506698GA17GENIChomozygous141289591
1190508519190508520CA19GENICheterozygous153897055
1190508687190508688AG18GENIChomozygous141289592
1190509515190509516TC12GENIChomozygous141289593
1190509640190509641AC22GENIChomozygous141289594
1190510265190510266AG10GENIChomozygous141289595
1190510565190510566CT12GENIChomozygous141289596
1190512254190512255AG21GENIChomozygous141289597
1190513540190513541CG16GENIChomozygous141289598
1190514350190514351AG22GENIChomozygous141289599
1190514823190514824CG12GENIChomozygous141289600
1190514823190514824C12GENICheterozygous402976468
1190514984190514985TA23GENIChomozygous141289601
1190515068190515069TC17GENIChomozygous141289602
1190515185190515185AGAGGGCATCTATCCCATTAC20GENIChomozygous141177611
1190508519190508520C19GENIChomozygous141177608
1190509232190509232GT15GENIChomozygous141177609
1190511563190511563ATGGCCCTATGGTGTGTC19GENIChomozygous141177610
1190515267190515268CA16GENIChomozygous141289603
1190516056190516057GA10GENIChomozygous141289604
1190516914190516915TC14GENICpossibly homozygous141289605
1190522609190522610CT7GENIChomozygous135772865
1190522674190522675AG8GENIChomozygous135772866
1190522783190522784GC7GENIChomozygous141289606
1190522789190522790CT6GENIChomozygous141289607