chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117393680173936801GGCGGT19GENIChomozygous134234002
117393885873938859GC43GENIChomozygous115990387
117393919573939196AG46GENIChomozygous116248206
117393993973939940TA47GENIChomozygous115990389
117394020673940207CT44GENIChomozygous116248208
117394112373941123A29GENICheterozygous131480610
117394115773941158GT38GENIChomozygous115990393
117394277773942778CT52GENIChomozygous115990399
117394129473941295GT57GENICpossibly homozygous116054341
117394130673941307CT58GENICpossibly homozygous116054343
117394412773944127TGT32GENIChomozygous131480611
117394418173944182CT56GENIChomozygous116248210
117394449173944588GCCAACAGTGCTTTTTTTTTTTTTTTTTTTTTTTTGCCTGTTTTTCAAGATAGGGAGCCCCTGCATAGTCTTAGAATTCACTCTGAAGACCAGGTTG24GENIChomozygous131480612
117394775373947754TC37GENIChomozygous116248212
117394899173948992CT34GENIChomozygous116248214
117394937973949380TA50GENIChomozygous116248216
117395019473950195TC14GENIChomozygous116267120
117395147373951474GA47GENIChomozygous115990407
117395299873952999TC49GENIChomozygous116248218
117395348973953490CT40GENIChomozygous116248220
117395358173953582GA52GENIChomozygous115990409
117395605373956054CT46GENIChomozygous116308702
117395697473956975CT51GENIChomozygous115990413
117395797373957974G22GENIChomozygous131480619
117395354973953550GA50GENIChomozygous116248222
117396011873960119TA36GENICpossibly homozygous115990415
117396111273961113GA49GENIChomozygous116248224
117396124273961243AG43GENIChomozygous115990421
117396140873961409GA39GENIChomozygous116248226
117396197873961979CT31GENIChomozygous116248228
117396219173962192GA43GENIChomozygous115990423
117396228873962289GA43GENIChomozygous115990425
117396262873962629TA44GENICpossibly homozygous115990427
117396325873963259TG61GENIChomozygous115990429
117396384173963841T56GENICpossibly homozygous131480621