| ID: 127816160 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:131465059-131465598 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128702396..128703319) | | |
| ID: 127816159 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:131449798-131450674 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128687519..128688395) | | |
| ID: 127816158 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:131445872-131446509 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128683593..128684230) | | |
| ID: 127816157 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:131445235-131445871 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128682956..128683592) | | |
| ID: 127816156 | H3K4me1 hESC enhancer GRCh37_chr9:131430084-131430584 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128667805..128668305) | | |
| ID: 127816155 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:131419183-131419826 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128656877..128657547) | | |
| ID: 127816154 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:131418538-131419182 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128656259..128656903) | | |
| ID: 127816153 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:131403137-131403741 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128640858..128641462) | | |
| ID: 127816152 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:131398224-131398974 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128635945..128636695) | | |
| ID: 127816151 | H3K4me1 hESC enhancer GRCh37_chr9:131389301-131389946 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128627022..128627667) | | |
| ID: 127816150 | NANOG-H3K27ac hESC enhancer GRCh37_chr9:131317315-131317814 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128555036..128555535) | | |
| ID: 126860772 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr9:131396972-131398171 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128634693..128635892) | | |
| ID: 100506080 | high mobility group AT-hook 1 pseudogene 4 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128663134..128663578, complement) | | |
| ID: 100422540 | vesicle transport through interaction with t-SNAREs 1B pseudogene 4 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128650998..128652150) | | |
| ID: 89891 | dynein 2 intermediate chain 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128633653..128684460, complement) | CFAP133, DIC5, FAP133, SRTD11, WDR34, bA216B9.3 | 613363 |
| ID: 29941 | protein kinase N3 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128702503..128720916) | UTDP4-1 | 610714 |
| ID: 6709 | spectrin alpha, non-erythrocytic 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128552587..128633662) | DEE5, DEVEP, EIEE5, HMN11, HMND11, NEAS, SPG91, SPTA2 | 182810 |
| ID: 6418 | SET nuclear proto-oncogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128683424..128696396) | 2PP2A, I2PP2A, IGAAD, IPP2A2, MRD58, PHAPII, TAF-I, TAF-IBETA | 600960 |