chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1267608381267608382TC10GENIChomozygous61200961
1267608865267608866GA12GENICheterozygous61200963
1267609078267609083AGTGG-----9GENICpossibly homozygous61200965
1267609122267609123T-9GENIChomozygous61200969
1267609168267609169GA2GENICheterozygous61200971
1267609295267609296GGC4GENICheterozygous61200973
1267609303267609304TA8GENIChomozygous61200975
1267609886267609887GA3GENIChomozygous61200977
1267610104267610105GA13GENIChomozygous61200979
1267610445267610446AG16GENIChomozygous61200981
1267610465267610466TA17GENIChomozygous61200983
1267612402267612403CT16GENIChomozygous61200987
1267612680267612681AG11GENIChomozygous61200989
1267613195267613196TTTTC5GENIChomozygous61200991
1267613531267613532AT11GENICpossibly homozygous61200993
1267613647267613648GC6GENIChomozygous61200995
1267614275267614276AT3GENIChomozygous61201001
1267614355267614356CT13GENICpossibly homozygous61201003
1267614367267614368CG12GENIChomozygous61201005
1267615009267615010GC11GENICpossibly homozygous61201007
1267616354267616355GA14GENIChomozygous61201011
1267616383267616384CT14GENIChomozygous61201013
1267616569267616570CT24GENIChomozygous61201015