| ID: 127815349 | H3K4me1 hESC enhancer GRCh37_chr9:98104577-98105078 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95342295..95342796) | | |
| ID: 127815348 | OCT4 hESC enhancer GRCh37_chr9:98103789-98104290 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95341507..95342008) | | |
| ID: 127815347 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:97900452-97901082 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95138170..95138919) | | |
| ID: 127815346 | H3K4me1 hESC enhancer GRCh37_chr9:97894463-97894965 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95132181..95132683) | | |
| ID: 127815345 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:97865305-97865951 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95103023..95103669) | | |
| ID: 127815344 | H3K4me1 hESC enhancer GRCh37_chr9:97863941-97864440 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95101659..95102158) | | |
| ID: 127815343 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:97853735-97854484 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95091453..95092202) | | |
| ID: 127815342 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:97852985-97853734 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95090703..95091452) | | |
| ID: 124902339 | small nucleolar RNA U13 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95172495..95172598, complement) | | |
| ID: 124310598 | Sharpr-MPRA regulatory region 1693 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95268727..95269021) | | |
| ID: 124310597 | Sharpr-MPRA regulatory region 1665 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95193107..95193401) | | |
| ID: 124310596 | Sharpr-MPRA regulatory region 8238 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95131367..95131661) | | |
| ID: 124310595 | Sharpr-MPRA regulatory region 10736 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95129927..95130221) | | |
| ID: 107987102 | uncharacterized LOC107987102 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95106468..95108746) | | |
| ID: 100873541 | RNA, 5S ribosomal pseudogene 288 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95142449..95142541, complement) | RN5S288 | |
| ID: 100271238 | ribosomal protein S26 pseudogene 37 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95123501..95123938) | RPS26_12_999 | |
| ID: 643342 | ATM interactor pseudogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95292309..95295007) | | |
| ID: 84909 | aminopeptidase O (putative) [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94726699..95150224) | AP-O, APO, C90RF3, C9orf3, DYT31, ONPEP | 619600 |
| ID: 2176 | FA complementation group C [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95099054..95317709, complement) | FA3, FAC, FACC | 613899 |