chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117042314117042315GT20GENICpossibly homozygous115846155
7117043615117043616TC20GENIChomozygous115846157
7117046238117046239TG21GENIChomozygous115846159
7117046634117046635TG12GENIChomozygous115846175
7117046642117046643GC14GENIChomozygous115846177
7117046643117046644TA14GENIChomozygous115846179
7117047260117047260TTTTTC9GENICheterozygous129939101
7117048001117048002TC17GENIChomozygous115846181
7117048325117048325A11GENICpossibly homozygous128510431
7117046278117046279A16GENIChomozygous128510429
7117046396117046516GGCCTTGCTGGAGTAGGTGAGGCCTTGCTGGAGTAGGTGTGGCCTTGCTGGAGTAGATGAGGCCTTGCTGGAGTAGGTGAGGCCTTGCTGGAGTAGGTGTGGCCTTGCTGGAGTAGATGA14GENIChomozygous128510430
7117048750117048751GA16GENICpossibly homozygous115846183
7117049276117049278TC10GENICheterozygous128510432
7117049548117049549A8GENIChomozygous128510433
7117050030117050032TA14GENIChomozygous128510434
7117050309117050310TC22GENIChomozygous115846185
7117050544117050545AG22GENIChomozygous115846187
7117051060117051061A8GENIChomozygous128510435
7117051084117051085GA10GENIChomozygous115846189
7117051518117051519CT22GENICheterozygous115846191
7117051731117051732GA32GENIChomozygous115846193
7117051766117051766AT32GENICheterozygous128510436
7117052063117052063T7GENICheterozygous128510437
7117052103117052104GA7GENIChomozygous115846195
7117052654117052654AGAGA13GENIChomozygous128510438
7117053228117053229GA15GENIChomozygous115846197
7117053322117053323CT16GENIChomozygous115846199
7117053942117053942C20GENICpossibly homozygous128510439
7117054348117054349AG18GENIChomozygous115846201
7117054480117054481G13GENIChomozygous128510440
7117058574117058575GA15GENIChomozygous115846203
7117061618117061619GA24GENIChomozygous115846205
7117054380117054381GT14GENIChomozygous118258905
7117054379117054380GT14GENIChomozygous116301967
7117051406117051407AT22GENICheterozygous116224751