chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4177278583177278583AGGGAGA17GENIChomozygous128108821
4177287247177287248C30GENIChomozygous128108825
4177287251177287251A30GENIChomozygous128108826
4177287256177287256A29GENIChomozygous128108827
4177287263177287264G29GENIChomozygous128108828
4177287267177287267G29GENIChomozygous128108829
4177287289177287290T28GENIChomozygous128108830
4177287295177287295A28GENIChomozygous128108831
4177287306177287307C26GENIChomozygous128108832
4177287349177287350C22GENIChomozygous128108833
4177287351177287353AG22GENIChomozygous128108834
4177287383177287384A15GENIChomozygous128108835
4177287388177287388C17GENIChomozygous128108836
4177287398177287398A17GENIChomozygous128108837
4177287401177287404AAG15GENIChomozygous128108838
4177287430177287431C16GENIChomozygous128108839
4177287498177287499G12GENIChomozygous130547484
4177287507177287507A11GENIChomozygous130547485
4177287523177287523A10GENIChomozygous130547486
4177287529177287530C10GENIChomozygous130547487
4177287545177287546T6GENIChomozygous130547488
4177287550177287551C6GENIChomozygous130547489
4177287574177287574CTC5GENIChomozygous130547492
4177287555177287555CT6GENIChomozygous130547490
4177287570177287571T6GENIChomozygous130547491
4177287581177287581CT4GENIChomozygous130547493
4177287597177287603ACTTCT6GENIChomozygous130547494
4177287642177287643C9GENIChomozygous130547495
4177287647177287648G9GENIChomozygous130547496
4177287674177287674G13GENIChomozygous128108840
4177287699177287700G14GENIChomozygous128108841
4177287749177287749A23GENIChomozygous128108842
4177287774177287774C23GENIChomozygous128108843
4177287791177287792T21GENIChomozygous128108844
4177287810177287810C22GENIChomozygous128108845
4177287839177287841TG23GENIChomozygous128108846
4177287858177287859G22GENIChomozygous128108847
4177287897177287898A16GENIChomozygous128108848
4177311627177311627A24GENICheterozygous129905798
4177287613177287614TC5GENIChomozygous130550446