chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7115960929115960930GA28GENIChomozygous54831651
7115962091115962092GGCTGTGCTCTCTGAGGTGCCAGAGAGCTTTCACAGGAGTATCGATATTCACAA43GENIChomozygous55144590
7115962267115962268TC20GENIChomozygous54072466
7115962305115962306TTTGCTGCTGCTGCTGCTGCTGCTGCTGCTGC10GENIChomozygous55953129
7115962325115962326GC25GENIChomozygous54072470
7115963331115963332CT25GENIChomozygous54831657
7115963820115963821CT11GENIChomozygous54831659
7115963982115963983CT24GENIChomozygous54831661
7115964003115964004GA21GENIChomozygous54831663
7115964779115964780TC22GENIChomozygous54831665
7115965749115965750GC16GENIChomozygous54072476
7115966667115966668C-31GENIChomozygous54072481
7115967523115967524C-14GENIChomozygous54831667
7115967624115967625GA14GENIChomozygous54831669
7115967756115967757C-25GENIChomozygous54072487
7115967757115967758CG25GENIChomozygous54920529
7115968027115968028CCT14GENIChomozygous54072489
7115970356115970358TG--21GENICheterozygous54920533
7115970359115970360AAG22GENICheterozygous54920535
7115970534115970535TTATATATATATATACAC4GENIChomozygous54999505
7115970701115970702TTAA12GENIChomozygous54831678
7115971178115971179TTTGTG11GENIChomozygous55144591
7115971213115971214CT13GENIChomozygous55144592
7115971217115971218CT17GENIChomozygous55144593
7115971495115971496CT18GENIChomozygous54831680
7115971693115971694CT19GENIChomozygous54831682
7115971714115971715CT17GENIChomozygous54831684
7115971788115971789CCA8GENIChomozygous54831686
7115971796115971797CA9GENIChomozygous55144594
7115971860115971861AAT11GENIChomozygous54831688
7115972153115972154AG21GENIChomozygous54072510
7115972186115972187CT20GENIChomozygous54831692
7115973607115973608GC3GENIChomozygous55132280
7115973619115973620GC3GENIChomozygous55953130
7115973629115973630GC2GENIChomozygous55953131
7115974751115974752TG28GENIChomozygous54831694
7115975196115975197TC20GENIChomozygous54831696
7115975271115975272TC13GENIChomozygous54072522
7115975337115975338TC14GENIChomozygous54072524