chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145264840145264841TC21INTERGENIChomozygous56967032
4145264959145264960GT11INTERGENICpossibly homozygous56967033
4145265041145265045TGTT----12INTERGENIChomozygous56967034
4145265203145265204TC21INTERGENICpossibly homozygous56967035
4145266273145266274AG16INTERGENIChomozygous56967036
4145266319145266321TT--7INTERGENIChomozygous56967037
4145267253145267254CG11INTERGENICheterozygous56967038
4145268861145268862AC22INTERGENIChomozygous56967039
4145269619145269620AG16INTERGENICpossibly homozygous56967040
4145269747145269748GA24INTERGENICpossibly homozygous56967041
4145270152145270153CT21INTERGENICpossibly homozygous56967042
4145270880145270881CT16INTERGENICpossibly homozygous56967046
4145271825145271826AC13INTERGENICpossibly homozygous56967047
4145272280145272281CT19INTERGENIChomozygous56967048
4145272496145272497TC11INTERGENIChomozygous56967049
4145272573145272574A-12INTERGENICpossibly homozygous56967050
4145273041145273042GA22INTERGENIChomozygous56967051
4145274093145274094CT19INTERGENICheterozygous56967052
4145274448145274449T-13INTERGENIChomozygous56967053
4145274543145274544TC16INTERGENIChomozygous56967054
4145275203145275204GT15INTERGENIChomozygous56967055
4145275642145275643AG13INTERGENICheterozygous56967057
4145275740145275741TC18INTERGENICpossibly homozygous56967058
4145275773145275774TTG14INTERGENICpossibly homozygous56967059
4145275795145275796AG12INTERGENIChomozygous56967060
4145275838145275839AG25INTERGENIChomozygous56967062
4145277100145277101TC21INTERGENICpossibly homozygous56967063
4145277365145277366AC11INTERGENICpossibly homozygous56967064
4145277647145277648TC20INTERGENICpossibly homozygous56967065
4145278279145278280GT8INTERGENICheterozygous56967066
4145280486145280487CG20INTERGENICpossibly homozygous56967068
4145278284145278285AG4INTERGENICheterozygous58285153