chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1267608381267608382TC23GENIChomozygous61200961
1267608865267608866GA24GENIChomozygous61200963
1267609078267609083AGTGG-----24GENIChomozygous61200965
1267609122267609123T-22GENIChomozygous61200969
1267609168267609169GA24GENIChomozygous61200971
1267609295267609296GGC23GENIChomozygous61200973
1267609303267609304TA27GENIChomozygous61200975
1267609886267609887GA13GENIChomozygous61200977
1267610104267610105GA24GENIChomozygous61200979
1267610445267610446AG17GENIChomozygous61200981
1267610465267610466TA18GENIChomozygous61200983
1267611177267611179TT--14GENICpossibly homozygous61200985
1267611180267611181T-14GENICheterozygous61642181
1267612402267612403CT21GENICpossibly homozygous61200987
1267612680267612681AG20GENIChomozygous61200989
1267613195267613196TTTTC17GENIChomozygous61200991
1267613531267613532AT28GENIChomozygous61200993
1267613647267613648GC27GENIChomozygous61200995
1267613824267613825T-9GENIChomozygous61200997
1267613849267613850GGA15GENIChomozygous61200999
1267614275267614276AT11GENIChomozygous61201001
1267614355267614356CT13GENIChomozygous61201003
1267614367267614368CG13GENIChomozygous61201005
1267615009267615010GC36GENIChomozygous61201007
1267615227267615228T-13GENIChomozygous61201009
1267616354267616355GA33GENIChomozygous61201011
1267616383267616384CT31GENIChomozygous61201013
1267616569267616570CT34GENIChomozygous61201015