chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69374046293740463AG15GENIChomozygous114904749
69374125193741252C27GENICpossibly homozygous128367987
69374279293742793AC37GENIChomozygous114904751
69374306293743071TTATTATCG25GENIChomozygous128367988
69374337193743371C18GENIChomozygous128367989
69374576593745766AT31GENIChomozygous114904753
69374578093745782AA28GENIChomozygous128367990
69374578793745787A28GENIChomozygous128367991
69374578993745789A29GENIChomozygous128367992
69374581393745814G33GENIChomozygous128367993
69374582593745825T34GENIChomozygous128367994
69374429993744300TC3GENIChomozygous126358331
69374430593744306AC4GENIChomozygous126358333
69374502193745022GC6GENICheterozygous126358335
69374509993745100TC5GENICheterozygous126358337
69374522693745227TC7GENIChomozygous126358339
69374592393745924G37GENIChomozygous128367995
69374593193745931A38GENIChomozygous128367996
69374597493745975AC37GENIChomozygous114904755
69374597793745978AT35GENIChomozygous114904757
69374597993745980CG35GENIChomozygous114904759
69374598093745981CG35GENIChomozygous114904761
69374617193746171C31GENIChomozygous128367997
69374617593746181ACTTAA30GENIChomozygous128367998
69374664093746640ATGGTTGTGAGCCACCATGTGGTTGCTAGGAATTGAACTCAGGACCTCTGGAAGAGCAGTCAGTGCTCTTAACCACTGAGTCATCTCTCC17GENIChomozygous128367999
69374722093747221TG44GENIChomozygous114904763
69374738093747382CT37GENIChomozygous128368000
69374759493747595CT48GENIChomozygous114904767
69374784593747846AG34GENIChomozygous114904769
69374785693747857AG32GENIChomozygous114904771
69374914893749149TC55GENIChomozygous114904773
69375006693750067GA49GENIChomozygous114904775
69375054593750546GT41GENIChomozygous114904777
69374617193746172TA30GENIChomozygous118554921
69374738493747385TA38GENIChomozygous118554922