chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103066042530660426GC8GENIChomozygous51389267
103066044930660450TA7GENIChomozygous51389268
103066045130660452CA7GENIChomozygous51389269
103066046430660465TG6GENIChomozygous53514207
103066046830660469CG5GENIChomozygous53514209
103066047230660473TG5GENIChomozygous51389270
103067742730677435ACTGCAAG--------17GENICheterozygous52491314
103067812430678125AG17GENIChomozygous51389333
103067820530678206TC28GENIChomozygous51389334
103067827730678278CA16GENIChomozygous51389335
103067833630678337CT13GENIChomozygous51389336
103068235330682354TTC9GENIChomozygous51389340
103068236330682364GA9GENIChomozygous53514211
103068236430682365TG10GENIChomozygous53514213
103068237530682376GA11GENIChomozygous51389341
103068339530683396CCTG11GENIChomozygous52491318
103069789830697899GGATGA13GENIChomozygous52315882
103071178030711781C-7GENIChomozygous51389441
103071973830719739TTCA14GENIChomozygous51389506
103072586830725869GGACT10GENIChomozygous51389560
103073408430734092AGAAAGAA--------7GENICheterozygous53514215
103073504630735048TG--11GENIChomozygous51389612
103074723630747237TA24GENICheterozygous53514217
103074726930747270A-29GENICheterozygous52364797
103074727730747278CA29GENICheterozygous53514219
103074728730747288CT27GENICheterozygous53514221
103074729730747298CG26GENICheterozygous53514223
103074730130747302AG31GENICheterozygous53514225
103075092630750927GA14GENICheterozygous53514227
103075093030750931GA14GENICheterozygous53514229
103075586730755868AC15GENIChomozygous51389749
103075592430755925TG10GENIChomozygous51389750
103075592530755926CG10GENIChomozygous51389751
103075592730755928CT10GENIChomozygous51633726
103075592830755929TG10GENIChomozygous51633727
103077168330771684T-9GENICheterozygous53514231
103078470030784701TA18GENIChomozygous51389834
103082945530829456T-20GENICheterozygous51389914