chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7115962267115962268TC23GENIChomozygous54072466
7115962305115962306TTTGCTGCTGCTGCTGC12GENIChomozygous54999503
7115962325115962326GC28GENIChomozygous54072470
7115962403115962404TC25GENIChomozygous54072472
7115965123115965124CT51GENIChomozygous54072474
7115965749115965750GC26GENIChomozygous54072476
7115965951115965952CCAGCT8GENIChomozygous54920525
7115966030115966058CTCTCCCTCTCCCTCTCCCTCTCCCTCT----------------------------4GENIChomozygous54920527
7115966667115966668C-15GENIChomozygous54072481
7115966838115966839GA22GENIChomozygous54072483
7115967522115967524CC--23GENIChomozygous54072485
7115967756115967757C-27GENIChomozygous54072487
7115967757115967758CG27GENIChomozygous54920529
7115968035115968036TC19GENIChomozygous54920531
7115970356115970358TG--19GENICheterozygous54920533
7115970359115970360AAG17GENICheterozygous54920535
7115970394115970395GA13GENICpossibly homozygous54072499
7115970534115970535TTATATATATATATACAC8GENIChomozygous54999505
7115970702115970703A-19GENIChomozygous54072501
7115971178115971179TTTGTGTGTGTGTG6GENICheterozygous54999509
7115970873115970874TC18GENIChomozygous54072503
7115971146115971148CT--20GENIChomozygous54072504
7115971178115971179TTTGTGTGTGTG6GENICheterozygous54999507
7115972153115972154AG19GENIChomozygous54072510
7115972276115972277GC21GENIChomozygous54072512
7115973579115973580GGTCTCTC15GENIChomozygous54072514
7115973613115973614CG26GENIChomozygous54072516
7115973665115973666CG21GENIChomozygous54072518
7115975271115975272TC23GENICpossibly homozygous54072522
7115975337115975338TC31GENIChomozygous54072524