chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174739762047397621CA11GENIChomozygous111057317
174740075947400760AG25GENIChomozygous111057318
174740090647400907TC24GENIChomozygous111057319
174740317347403174TA9GENIChomozygous111057320
174740377047403771GC15GENIChomozygous111057321
174740383347403834AG13GENIChomozygous111057322
174740491347404914GC8GENIChomozygous111057323
174740579947405800TC18GENICheterozygous111057324
174740691447406915CA4GENICheterozygous125625451
174740697247406973CT18GENIChomozygous111057325
174740803147408032CT27GENIChomozygous111057326
174740858547408586CT23GENIChomozygous111057327
174740911447409115TC14GENIChomozygous111057328
174740921847409219CT14GENIChomozygous111057329
174741050747410508AG15GENIChomozygous111057330
174741104347411044TC13GENIChomozygous111057331
174741120547411206TC15GENIChomozygous111057332
174741266147412662AT13GENIChomozygous111057333
174741367647413677CT16GENIChomozygous111057334
174741374247413743TC17GENIChomozygous111057335
174741559647415597AT16GENIChomozygous111057336
174741596247415963GA18GENIChomozygous111057337
174741648447416485AC18GENIChomozygous111057338
174741694947416950GT14GENIChomozygous111057339
174741727747417278AG22GENIChomozygous111057340
174741814247418143TG14GENIChomozygous111057341
174741890047418901TG28GENIChomozygous111057342
174741893847418939TA12GENIChomozygous111057343
174741939447419395GT12GENIChomozygous111057344
174741977847419779CT20GENIChomozygous111057345
174742022447420225CG24GENIChomozygous111057346