| ID: 130002296 | ATAC-STARR-seq lymphoblastoid silent region 20156 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107283258..107283817) | | |
| ID: 130002295 | ATAC-STARR-seq lymphoblastoid active region 28750 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107282608..107282767) | | |
| ID: 130002294 | ATAC-STARR-seq lymphoblastoid active region 28749 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107219157..107219216) | | |
| ID: 127815553 | NANOG-H3K27ac hESC enhancer GRCh37_chr9:110200480-110201150 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107438199..107438869) | | |
| ID: 127815552 | H3K27ac hESC enhancer GRCh37_chr9:110199139-110199809 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107436858..107437528) | | |
| ID: 127815551 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:110020689-110021228 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107258408..107258947) | | |
| ID: 127815550 | NANOG-H3K27ac hESC enhancer GRCh37_chr9:110011081-110012047 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107248800..107249766) | | |
| ID: 126860718 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr9:110005805-110007004 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107243524..107244723) | | |
| ID: 124906804 | uncharacterized LOC124906804 [Homo sapiens (human)] | | | |
| ID: 124906803 | importin subunit alpha-1-like [Homo sapiens (human)] | | | |
| ID: 124902241 | uncharacterized LOC124902241 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107340207..107343225) | | |
| ID: 121331341 | Sharpr-MPRA regulatory region 15312 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107341128..107341422) | | |
| ID: 107987111 | uncharacterized LOC107987111 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107363715..107383457) | | |
| ID: 107987110 | uncharacterized LOC107987110 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107222237..107232139) | | |
| ID: 101928720 | long intergenic non-protein coding RNA 1509 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107420284..107466585, complement) | PRCAT37 | |
| ID: 100874473 | high mobility group nucleosomal binding domain 2 pseudogene 32 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107457942..107458438, complement) | | |
| ID: 644661 | importin subunit alpha-1-like [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107169125..107171142, complement) | | |
| ID: 5887 | RAD23 homolog B, nucleotide excision repair protein [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107283279..107332194) | HHR23B, HR23B, P58 | 600062 |