chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117042314117042315GT52GENIChomozygous115846155
7117043615117043616TC58GENIChomozygous115846157
7117046238117046239TG39GENIChomozygous115846159
7117046634117046635TG33GENIChomozygous115846175
7117046642117046643GC35GENIChomozygous115846177
7117046643117046644TA35GENIChomozygous115846179
7117048001117048002TC37GENIChomozygous115846181
7117048750117048751GA38GENIChomozygous115846183
7117048325117048325A43GENICpossibly homozygous128510431
7117049548117049549A32GENICpossibly homozygous128510433
7117046278117046279A37GENIChomozygous128510429
7117046396117046516GGCCTTGCTGGAGTAGGTGAGGCCTTGCTGGAGTAGGTGTGGCCTTGCTGGAGTAGATGAGGCCTTGCTGGAGTAGGTGAGGCCTTGCTGGAGTAGGTGTGGCCTTGCTGGAGTAGATGA32GENIChomozygous128510430
7117049276117049278TC35GENICpossibly homozygous128510432
7117047260117047260TTTTTC20GENICheterozygous129939101
7117050030117050032TA40GENIChomozygous128510434
7117050309117050310TC44GENIChomozygous115846185
7117050544117050545AG57GENIChomozygous115846187
7117051060117051061A29GENIChomozygous128510435
7117051084117051085GA38GENIChomozygous115846189
7117051518117051519CT66GENICheterozygous115846191
7117051731117051732GA64GENIChomozygous115846193
7117051766117051766AT80GENICheterozygous128510436
7117052103117052104GA42GENIChomozygous115846195
7117052654117052654AGAGA29GENIChomozygous128510438
7117053228117053229GA46GENIChomozygous115846197
7117053322117053323CT50GENIChomozygous115846199
7117053942117053942C47GENIChomozygous128510439
7117054348117054349AG35GENIChomozygous115846201
7117054480117054481G52GENIChomozygous128510440
7117058574117058575GA55GENIChomozygous115846203
7117061618117061619GA44GENIChomozygous115846205
7117054380117054381GT31GENIChomozygous118258905
7117051271117051272AG53GENICheterozygous128562334
7117054379117054380GT32GENIChomozygous116301967
7117051406117051407AT45GENICheterozygous116224751