chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7110725452110725453GA32GENIChomozygous138181611
7110726144110726145TC32GENIChomozygous138181612
7110727712110727713CT22GENIChomozygous138181614
7110727810110727811AG22GENIChomozygous138181615
7110727916110727917AG16GENIChomozygous138181616
7110728499110728500AG31GENIChomozygous138181617
7110728591110728592GC22GENIChomozygous138181619
7110729130110729131TC20GENIChomozygous138181621
7110729373110729374AG26GENIChomozygous138181622
7110729983110729984AG41GENIChomozygous138181623
7110730425110730426GA26GENIChomozygous138181624
7110731139110731140GA21GENIChomozygous143365413
7110731952110731953TC30GENIChomozygous138181626
7110732886110732886CAGCTAGAC23GENIChomozygous137974146
7110733000110733001TC26GENIChomozygous138181627
7110733126110733127TC17GENIChomozygous138181628
7110733147110733148TG16GENIChomozygous138181629
7110733164110733279CCTAAATCTGTCTTCTTTTTTGGTTCTTTTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCCT19GENIChomozygous137974147
7110733644110733645TC34GENIChomozygous138181630
7110734150110734151T17GENICheterozygous403617303
7110734150110734151TG17GENICheterozygous403617304