chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1267608381267608382TC17GENIChomozygous61200961
1267608865267608866GA10GENIChomozygous61200963
1267609078267609083AGTGG-----20GENIChomozygous61200965
1267609082267609083GGT19GENICheterozygous61200967
1267609122267609123T-12GENIChomozygous61200969
1267609168267609169GA15GENIChomozygous61200971
1267609295267609296GGC20GENIChomozygous61200973
1267609303267609304TA20GENIChomozygous61200975
1267609784267609785CT23GENIChomozygous61642180
1267609875267609876T-15GENICheterozygous61684431
1267610104267610105GA21GENIChomozygous61200979
1267610445267610446AG20GENIChomozygous61200981
1267610465267610466TA17GENIChomozygous61200983
1267611177267611179TT--14GENICpossibly homozygous61200985
1267611180267611181T-12GENICheterozygous61642181
1267612402267612403CT11GENIChomozygous61200987
1267612680267612681AG20GENIChomozygous61200989
1267612917267612918GA13GENIChomozygous61642182
1267613195267613196TTTTC18GENIChomozygous61200991
1267613531267613532AT21GENIChomozygous61200993
1267613598267613600CT--20GENIChomozygous61642183
1267613647267613648GC15GENIChomozygous61200995
1267613824267613825T-5GENIChomozygous61200997
1267613849267613850GGA6GENIChomozygous61200999
1267614275267614276AT4GENIChomozygous61201001
1267614355267614356CT13GENIChomozygous61201003
1267614367267614368CG9GENIChomozygous61201005
1267615009267615010GC27GENIChomozygous61201007
1267615227267615228T-12GENIChomozygous61201009
1267616383267616384CT21GENIChomozygous61201013
1267616569267616570CT17GENIChomozygous61201015