chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69374046293740463AG11GENIChomozygous114904749
69374125193741252C37GENIChomozygous128367987
69374279293742793AC44GENIChomozygous114904751
69374306293743071TTATTATCG31GENICpossibly homozygous128367988
69374337193743371C25GENIChomozygous128367989
69374429993744300TC5GENIChomozygous126358331
69374430593744306AC4GENIChomozygous126358333
69374502193745022GC4GENIChomozygous126358335
69374509993745100TC6GENIChomozygous126358337
69374578093745782AA45GENIChomozygous128367990
69374578793745787A43GENIChomozygous128367991
69374578993745789A46GENIChomozygous128367992
69374581393745814G45GENIChomozygous128367993
69374582593745825T46GENIChomozygous128367994
69374592393745924G46GENIChomozygous128367995
69374593193745931A45GENIChomozygous128367996
69374598093745981CG41GENIChomozygous114904761
69374522693745227TC15GENIChomozygous126358339
69374576593745766AT40GENIChomozygous114904753
69374597493745975AC40GENIChomozygous114904755
69374597793745978AT41GENIChomozygous114904757
69374597993745980CG41GENIChomozygous114904759
69374617193746171C32GENIChomozygous128367997
69374617593746181ACTTAA30GENIChomozygous128367998
69374664093746640ATGGTTGTGAGCCACCATGTGGTTGCTAGGAATTGAACTCAGGACCTCTGGAAGAGCAGTCAGTGCTCTTAACCACTGAGTCATCTCTCC12GENIChomozygous128367999
69374722093747221TG54GENICpossibly homozygous114904763
69374738093747382CT59GENIChomozygous128368000
69374759493747595CT50GENIChomozygous114904767
69374784593747846AG59GENIChomozygous114904769
69374785693747857AG58GENIChomozygous114904771
69374914893749149TC48GENIChomozygous114904773
69375006693750067GA46GENIChomozygous114904775
69375054593750546GT48GENIChomozygous114904777
69374617193746172TA30GENIChomozygous118554921
69374738493747385TA61GENIChomozygous118554922