chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130135903130135904GA8GENIChomozygous115889328
7130135951130135952CT16GENIChomozygous115889330
7130136462130136463GA16GENIChomozygous116345890
7130136591130136592GA20GENIChomozygous116345892
7130137124130137125CT8GENIChomozygous115889332
7130137327130137328GA10GENIChomozygous115889336
7130137421130137422AG17GENIChomozygous115889338
7130138813130138814CT20GENIChomozygous116345896
7130141574130141575TC16GENIChomozygous115889342
7130145349130145350TC19GENIChomozygous115889346
7130145425130145426GA20GENIChomozygous115889348
7130145798130145799AG15GENIChomozygous115889352
7130146565130146566AG13GENIChomozygous115889356
7130148326130148327AG14GENIChomozygous115889360
7130149238130149239AG27GENIChomozygous115889364
7130149515130149516CT25GENIChomozygous115889366
7130149554130149555AG18GENIChomozygous115889368
7130149754130149755AG24GENIChomozygous115889370
7130150854130150855TG15GENIChomozygous115889374
7130152107130152108AG14GENIChomozygous115889380
7130152135130152136GA14GENIChomozygous115889382
7130153012130153013CT24GENIChomozygous116345898
7130153928130153929AG9GENIChomozygous115889386
7130155217130155218CT17GENIChomozygous115889388
7130157571130157572AG24GENIChomozygous115889392
7130157771130157772CG29GENIChomozygous115889396
7130157876130157877GA16GENIChomozygous116345900
7130158036130158037AC11GENIChomozygous115889398
7130158781130158782CT12GENIChomozygous115889402
7130159401130159402CT22GENIChomozygous115889404
7130160494130160495AG23GENIChomozygous116345902
7130161202130161203TG7GENIChomozygous116345904
7130161454130161455TC7GENIChomozygous115889414
7130160406130160407GA16GENIChomozygous115889408
7130160594130160595GC16GENIChomozygous115889410