chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1267608381267608382TC23GENIChomozygous61200961
1267608865267608866GA33GENIChomozygous61200963
1267609078267609083AGTGG-----31GENIChomozygous61200965
1267609122267609123T-37GENIChomozygous61200969
1267609168267609169GA29GENIChomozygous61200971
1267609295267609296GGC37GENIChomozygous61200973
1267609303267609304TA33GENIChomozygous61200975
1267609886267609887GA20GENIChomozygous61200977
1267610104267610105GA29GENIChomozygous61200979
1267610445267610446AG36GENIChomozygous61200981
1267610465267610466TA38GENIChomozygous61200983
1267611177267611179TT--15GENICpossibly homozygous61200985
1267612402267612403CT24GENIChomozygous61200987
1267612680267612681AG32GENIChomozygous61200989
1267613195267613196TTTTC30GENIChomozygous61200991
1267613531267613532AT40GENIChomozygous61200993
1267613647267613648GC27GENIChomozygous61200995
1267613824267613825T-35GENICpossibly homozygous61200997
1267613849267613850GGA37GENIChomozygous61200999
1267614275267614276AT30GENIChomozygous61201001
1267614355267614356CT15GENIChomozygous61201003
1267614367267614368CG22GENIChomozygous61201005
1267615009267615010GC29GENIChomozygous61201007
1267615227267615228T-18GENIChomozygous61201009
1267616354267616355GA41GENIChomozygous61201011
1267616383267616384CT32GENIChomozygous61201013
1267616569267616570CT34GENIChomozygous61201015