| ID: 127816297 | H3K4me1 hESC enhancer GRCh37_chr9:132999231-132999790 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130236952..130237511) | | |
| ID: 127816296 | H3K4me1 hESC enhancer GRCh37_chr9:132981410-132982372 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130219131..130220093) | | |
| ID: 127816295 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:132977599-132978255 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130215320..130215976) | | |
| ID: 127816294 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:132972653-132973344 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130210374..130211065) | | |
| ID: 127816293 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:132971269-132971960 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130208990..130209681) | | |
| ID: 127816292 | H3K27ac hESC enhancer GRCh37_chr9:132960001-132960500 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130197722..130198221) | | |
| ID: 127816291 | H3K27ac hESC enhancer GRCh37_chr9:132959499-132960000 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130197220..130197721) | | |
| ID: 127816290 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:132949630-132950471 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130187351..130188192) | | |
| ID: 127816289 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:132948787-132949629 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130186508..130187350) | | |
| ID: 127816288 | H3K4me1 hESC enhancer GRCh37_chr9:132947945-132948786 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130185666..130186507) | | |
| ID: 127816287 | H3K4me1 hESC enhancer GRCh37_chr9:132936047-132936957 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130173768..130174678) | | |
| ID: 127816286 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:132933797-132934585 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130171518..130172306) | | |
| ID: 127816285 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:132913067-132913905 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130150788..130151626) | | |
| ID: 124310667 | Sharpr-MPRA regulatory region 5428 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130216710..130217004) | | |
| ID: 113839530 | Sharpr-MPRA regulatory region 4503 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130240630..130240924) | | |
| ID: 113219459 | microRNA 12126 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130241387..130241488) | | |
| ID: 23413 | neuronal calcium sensor 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130172404..130237303) | FLUP, FREQ | 603315 |