chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7115960929115960930GA19GENIChomozygous54831651
7115962267115962268TC4GENICheterozygous54072466
7115962305115962306TTTGCTGCTGCTGCTGCTGCTGCTGCTGCTGC1GENIChomozygous55953129
7115962325115962326GC7GENIChomozygous54072470
7115963331115963332CT20GENICpossibly homozygous54831657
7115963820115963821CT15GENIChomozygous54831659
7115963982115963983CT12GENIChomozygous54831661
7115964003115964004GA13GENIChomozygous54831663
7115964779115964780TC22GENICpossibly homozygous54831665
7115965749115965750GC18GENICpossibly homozygous54072476
7115966667115966668C-15GENICpossibly homozygous54072481
7115967523115967524C-5GENIChomozygous54831667
7115967624115967625GA2GENIChomozygous54831669
7115967756115967757C-8GENIChomozygous54072487
7115967757115967758CG8GENIChomozygous54920529
7115970356115970358TG--26GENICheterozygous54920533
7115970359115970360AAG26GENICheterozygous54920535
7115971217115971218CT7GENICheterozygous55144593
7115971495115971496CT13GENIChomozygous54831680
7115971693115971694CT9GENICpossibly homozygous54831682
7115971714115971715CT5GENICheterozygous54831684
7115971788115971789CCA1GENIChomozygous54831686
7115971796115971797CA1GENIChomozygous55144594
7115971860115971861AAT1GENIChomozygous54831688
7115972153115972154AG5GENIChomozygous54072510
7115972186115972187CT9GENICheterozygous54831692
7115974751115974752TG23GENICpossibly homozygous54831694
7115975196115975197TC16GENICheterozygous54831696
7115975271115975272TC15GENIChomozygous54072522
7115975337115975338TC11GENIChomozygous54072524