ID: 127814460 | NANOG hESC enhancer GRCh37_chr9:16243838-16244339 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (16243840..16244341) | | |
ID: 127814459 | H3K4me1 hESC enhancer GRCh37_chr9:16179471-16179971 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (16179473..16179973) | | |
ID: 127814458 | H3K4me1 hESC enhancer GRCh37_chr9:15618475-15618974 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (15618477..15618976) | | |
ID: 127814457 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:15552638-15553283 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (15552640..15553350) | | |
ID: 127814456 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:15533117-15533656 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (15533119..15533658) | | |
ID: 126860584 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr9:16060174-16061373 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (16060176..16061375) | | |
ID: 126860583 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr9:16030074-16031273 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (16030076..16031275) | | |
ID: 124906800 | uncharacterized LOC124906800 [Homo sapiens (human)] | | | |
ID: 107987049 | uncharacterized LOC107987049 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (15784704..15785661) | | |
ID: 106481884 | RNA, U6 small nuclear 246, pseudogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (15544188..15544294) | | |
ID: 100873746 | RNA, U6 small nuclear 14, pseudogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (15776182..15776286, complement) | RNU6-14 | |
ID: 100129385 | long intergenic non-protein coding RNA 3041 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (16203935..16276313, complement) | C9orf92, Em:AL513424.1 | |
ID: 728234 | high mobility group nucleosomal binding domain 2 pseudogene 16 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (15588235..15588724) | HMGN2L | |
ID: 203238 | coiled-coil domain containing 171 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (15552885..16108926) | C9orf93, bA536D16.1, bA778P13.1 | |