chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1267608381267608382TC12GENIChomozygous61200961
1267608865267608866GA16GENIChomozygous61200963
1267609078267609083AGTGG-----10GENIChomozygous61200965
1267609082267609083GGT11GENICheterozygous61200967
1267609122267609123T-15GENIChomozygous61200969
1267609168267609169GA20GENIChomozygous61200971
1267609295267609296GGC13GENIChomozygous61200973
1267609303267609304TA14GENIChomozygous61200975
1267609886267609887GA21GENIChomozygous61200977
1267610104267610105GA15GENIChomozygous61200979
1267610445267610446AG21GENIChomozygous61200981
1267610465267610466TA22GENIChomozygous61200983
1267611177267611179TT--5GENIChomozygous61200985
1267612402267612403CT9GENIChomozygous61200987
1267612680267612681AG23GENIChomozygous61200989
1267613195267613196TTTTC14GENIChomozygous61200991
1267613531267613532AT14GENIChomozygous61200993
1267613647267613648GC25GENIChomozygous61200995
1267613824267613825T-5GENIChomozygous61200997
1267613849267613850GGA6GENIChomozygous61200999
1267614355267614356CT16GENIChomozygous61201003
1267614367267614368CG18GENIChomozygous61201005
1267615009267615010GC22GENIChomozygous61201007
1267615227267615228T-7GENIChomozygous61201009
1267616354267616355GA41GENIChomozygous61201011
1267616383267616384CT41GENIChomozygous61201013
1267616569267616570CT38GENIChomozygous61201015