chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117042314117042315GT17GENIChomozygous115846155
7117043615117043616TC7GENIChomozygous115846157
7117046238117046239TG15GENIChomozygous115846159
7117046634117046635TG13GENIChomozygous115846175
7117046642117046643GC10GENIChomozygous115846177
7117046643117046644TA10GENIChomozygous115846179
7117048001117048002TC20GENIChomozygous115846181
7117048325117048325A7GENICpossibly homozygous128510431
7117046278117046279A12GENIChomozygous128510429
7117047260117047260TTTTTC13GENICheterozygous129939101
7117048750117048751GA10GENIChomozygous115846183
7117049276117049278TC14GENICheterozygous128510432
7117049548117049549A17GENIChomozygous128510433
7117050030117050032TA13GENIChomozygous128510434
7117050309117050310TC7GENIChomozygous115846185
7117050544117050545AG9GENIChomozygous115846187
7117051060117051061A9GENIChomozygous128510435
7117051084117051085GA12GENIChomozygous115846189
7117051518117051519CT12GENICheterozygous115846191
7117051731117051732GA14GENIChomozygous115846193
7117051766117051766AT13GENICheterozygous128510436
7117052103117052104GA15GENIChomozygous115846195
7117052654117052654AGAGA14GENIChomozygous128510438
7117053228117053229GA15GENIChomozygous115846197
7117053322117053323CT17GENIChomozygous115846199
7117053942117053942C10GENIChomozygous128510439
7117054348117054349AG8GENIChomozygous115846201
7117054380117054381GT5GENIChomozygous118258905
7117058574117058575GA17GENIChomozygous115846203
7117061618117061619GA10GENIChomozygous115846205
7117054379117054380GT6GENIChomozygous116301967
7117054480117054481G7GENIChomozygous128510440