chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
178121218281212183GA12GENIChomozygous111113688
178121361781213618TC17GENIChomozygous111113689
178121546081215461TG4GENIChomozygous125626604
178121827581218276GC5GENIChomozygous111113691
178121976781219768AG10GENIChomozygous111113693
178122025381220254AG14GENIChomozygous111113697
178122270681222707CT19GENIChomozygous111113699
178122273081222731TC20GENIChomozygous111113700
178122374081223741CA19GENIChomozygous111113702
178122398681223987TA19GENIChomozygous111113704
178122447381224474AG21GENIChomozygous111113706
178122489281224893GC14GENIChomozygous111113707
178122501181225012GT15GENIChomozygous111113709
178122519581225196TC13GENIChomozygous111113711
178122584781225848CT18GENIChomozygous111113713
178122801781228018CT19GENIChomozygous111113714
178122844981228450TA20GENIChomozygous111113716
178123071181230712CT16GENIChomozygous111113717
178123689881236899AG15GENIChomozygous111113721
178123813281238133TA3GENICheterozygous125626605
178123827181238272TG14GENIChomozygous111113723
178123883181238832TC17GENIChomozygous111113725
178124040681240407GA5GENICheterozygous111113727
178124232281242323AG24GENIChomozygous111113729
178124403981244040AG17GENIChomozygous111113731
178124607581246076AG15GENIChomozygous111113733
178124779381247794GA12GENIChomozygous111113735
178124838881248389CT17GENIChomozygous111113736
178124974581249746AG16GENIChomozygous111113738
178125085881250859TC19GENIChomozygous111113740
178125202181252022GA18GENICpossibly homozygous111113742
178125250281252503GA19GENIChomozygous111113744