chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187043346270433463CT12GENIChomozygous64609123
187043349270433493TC21GENIChomozygous64259284
187043386270433863TC19GENIChomozygous64609126
187043535170435353AA20GENICheterozygous64609129
187043613870436139CT10GENIChomozygous64609132
187043629070436291TC19GENIChomozygous64259286
187043689570436896TG27GENICpossibly homozygous64609135
187043777870437779TA21GENIChomozygous64609138
187043846870438469GT10GENIChomozygous64609144
187043917670439177AG25GENIChomozygous64259287
187044050870440509TC13GENIChomozygous64609147
187044075570440756AG9GENIChomozygous64609150
187044171570441716TC18GENIChomozygous64259288
187044176770441768AG20GENIChomozygous64609153
187044319770443198AG13GENIChomozygous64609156
187044332870443329TC4GENIChomozygous64259289
187044388570443886GC26GENICpossibly homozygous64609159
187044464970444650CT10GENIChomozygous64259290
187044541170445412GA9GENIChomozygous64609162
187044578070445781TC18GENIChomozygous64609165
187044594270445943AG24GENIChomozygous64609168
187044605570446056CT23GENIChomozygous64259294
187044932870449329CT9GENIChomozygous64609170
187044933570449336CT10GENIChomozygous64609173
187045043670450436T20GENIChomozygous64732107
187043793870437938G15GENIChomozygous64732101
187044922170449222C5GENIChomozygous64732104
187045080970450810GA13GENIChomozygous64609179
187045185270451852G19GENIChomozygous64732110
187045307570453076AG25GENIChomozygous64259297
187045517970455180AC24GENIChomozygous64259298
187045612770456128AC10GENIChomozygous64259299
187045775370457755TG11GENICheterozygous64609185
187045806970458070GA15GENIChomozygous64609188
187045807070458071CA15GENIChomozygous64609191
187045808270458083TC14GENIChomozygous64259301
187045813470458135AG18GENIChomozygous64259302