| ID: 127815023 | H3K4me1 hESC enhancer GRCh37_chr9:84375421-84375922 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81760506..81761007) | | |
| ID: 127815022 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:84303773-84304487 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81688858..81689794) | | |
| ID: 127815021 | H3K4me1 hESC enhancer GRCh37_chr9:84278031-84278532 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81663116..81663617) | | |
| ID: 127815020 | NANOG hESC enhancer GRCh37_chr9:84238663-84239186 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81623748..81624271) | | |
| ID: 127815019 | NANOG-H3K4me1 hESC enhancer GRCh37_chr9:84237249-84237864 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81622334..81622949) | | |
| ID: 127815018 | NANOG hESC enhancer GRCh37_chr9:84236633-84237248 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81621718..81622333) | | |
| ID: 127815017 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr9:84210801-84211494 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81595886..81596579) | | |
| ID: 127815016 | H3K4me1 hESC enhancer GRCh37_chr9:84210105-84210800 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81595190..81595885) | | |
| ID: 127815015 | NANOG-H3K4me1 hESC enhancer GRCh37_chr9:84164162-84164662 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81549247..81549747) | | |
| ID: 126860655 | MED14-independent group 3 enhancer GRCh37_chr9:84207247-84208446 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81592332..81593531) | | |
| ID: 124310571 | Sharpr-MPRA regulatory region 7656 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81676094..81676388) | | |
| ID: 121811708 | Sharpr-MPRA regulatory region 9381 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81673374..81673668) | | |
| ID: 110121076 | VISTA enhancer hs1359 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81649280..81652035) | | |
| ID: 110120996 | VISTA enhancer hs1118 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81552436..81553261) | | |
| ID: 110120702 | VISTA enhancer hs556 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81684295..81685202) | | |
| ID: 106481507 | RNA, U6 small nuclear 1035, pseudogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81725243..81725349, complement) | | |
| ID: 105376106 | uncharacterized LOC105376106 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81587675..81590110) | | |
| ID: 101927502 | TLE1 divergent transcript [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81689713..81776900) | | |
| ID: 7088 | TLE family member 1, transcriptional corepressor [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (81583683..81689547, complement) | ESG, ESG1, GRG1, TLE-1 | 600189 |