chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2217530778217530779AG21GENIChomozygous620913904
2217531441217531442CT3GENIChomozygous620913905
2217531761217531762CT12GENIChomozygous620913906
2217531850217531851CT15GENIChomozygous620913907
2217531938217531939CCA3GENIChomozygous738971168
2217533101217533102AT24GENIChomozygous620913908
2217533487217533488CCT3GENICheterozygous738971171
2217533487217533488CCTT3GENICheterozygous738971172
2217533923217533927TCTC----10GENICpossibly homozygous738971174
2217534422217534423TG13GENIChomozygous620913909
2217535148217535149TC14GENIChomozygous620913910
2217535275217535276GC10GENIChomozygous620913911
2217535389217535390TC13GENIChomozygous620913912
2217536071217536072TC17GENIChomozygous620913913
2217536085217536086AG18GENIChomozygous620913914
2217536086217536087GA18GENIChomozygous620913915
2217536385217536388TTT---6GENIChomozygous738971175
2217536586217536587CCGTGTGT15GENIChomozygous738971177
2217536836217536837CT20GENIChomozygous620913916
2217536923217536924CT26GENICpossibly homozygous620913917
2217537424217537425TC17GENIChomozygous620913918
2217538354217538355GA23GENIChomozygous620913919
2217540938217540939TC30GENIChomozygous620913920
2217541440217541441CCT19GENIChomozygous738971178
2217541453217541454GGT19GENIChomozygous738971179
2217542272217542273TC22GENIChomozygous620913921
2217542661217542662AG31GENIChomozygous620913922
2217543304217543305AT21GENIChomozygous620913923
2217543447217543448TG30GENIChomozygous620913924
2217546112217546113GT16GENIChomozygous620913925
2217546433217546434AAT11GENIChomozygous738971180
2217546841217546842T-15GENICpossibly homozygous738971181