chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174739762047397621CA8GENIChomozygous111057317
174740075947400760AG23GENIChomozygous111057318
174740090647400907TC37GENIChomozygous111057319
174740317347403174TA31GENIChomozygous111057320
174740377047403771GC30GENIChomozygous111057321
174740383347403834AG25GENIChomozygous111057322
174740491347404914GC38GENIChomozygous111057323
174740579947405800TC21GENIChomozygous111057324
174740697247406973CT25GENIChomozygous111057325
174740803147408032CT27GENIChomozygous111057326
174740858547408586CT25GENIChomozygous111057327
174740911447409115TC29GENIChomozygous111057328
174740921847409219CT31GENIChomozygous111057329
174741050747410508AG42GENIChomozygous111057330
174741266147412662AT24GENIChomozygous111057333
174741367647413677CT31GENIChomozygous111057334
174741374247413743TC29GENIChomozygous111057335
174741559647415597AT34GENIChomozygous111057336
174741596247415963GA24GENIChomozygous111057337
174741648447416485AC37GENIChomozygous111057338
174741694947416950GT21GENIChomozygous111057339
174741727747417278AG32GENIChomozygous111057340
174741814247418143TG32GENIChomozygous111057341
174741890047418901TG29GENIChomozygous111057342
174741893847418939TA28GENIChomozygous111057343
174741939447419395GT27GENIChomozygous111057344
174741977847419779CT32GENIChomozygous111057345
174742022447420225CG36GENIChomozygous111057346