ID: 130003062 | ATAC-STARR-seq lymphoblastoid silent region 20563 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136949790..136950289) | | |
ID: 130003061 | ATAC-STARR-seq lymphoblastoid silent region 20562 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136949670..136949769) | | |
ID: 130003060 | ATAC-STARR-seq lymphoblastoid silent region 20561 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136944202..136944781) | | |
ID: 130003059 | ATAC-STARR-seq lymphoblastoid active region 29336 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136902333..136902792) | | |
ID: 130003058 | ATAC-STARR-seq lymphoblastoid active region 29335 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136901783..136902102) | | |
ID: 129662596 | ReSE screen-validated silencer GRCh37_chr9:139847365-139847546 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136952913..136953094) | | |
ID: 127816861 | H3K4me1 hESC enhancer GRCh37_chr9:139862921-139863420 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136968469..136968968) | | |
ID: 127816860 | H3K4me1 hESC enhancer GRCh37_chr9:139862419-139862920 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136967967..136968468) | | |
ID: 127816859 | H3K4me1 hESC enhancer GRCh37_chr9:139853309-139853809 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136958857..136959357) | | |
ID: 127816858 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:139837603-139838368 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136943151..136943916) | | |
ID: 127816857 | H3K4me1 hESC enhancer GRCh37_chr9:139832510-139833122 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136938058..136938670) | | |
ID: 127816856 | H3K4me1 hESC enhancer GRCh37_chr9:139831896-139832509 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136937444..136938057) | | |
ID: 127816855 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:139781665-139782400 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136887213..136887948) | | |
ID: 127816854 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:139780929-139781664 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136886291..136887212) | | |
ID: 101928638 | long intergenic non-protein coding RNA 2692 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136969412..136972884) | C9orf141, PRR31 | |
ID: 100616480 | microRNA 4479 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136886733..136886803) | | |
ID: 286256 | lipocalin 12 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136949197..136956538) | | 612905 |
ID: 54461 | F-box and WD repeat domain containing 5 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136940435..136944738, complement) | Fbw5 | 609072 |
ID: 7186 | TNF receptor associated factor 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136881958..136926607) | MGC:45012, RNF117, TRAP, TRAP3 | 601895 |
ID: 733 | complement C8 gamma chain [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136945243..136946975) | C8C | 120930 |