ID: 127814485 | H3K4me1 hESC enhancer GRCh37_chr9:17539955-17540454 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17539957..17540456) | | |
ID: 127814484 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:17353653-17354168 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17353655..17354170) | | |
ID: 127814483 | OCT4-NANOG hESC enhancer GRCh37_chr9:17332022-17332668 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17332024..17332670) | | |
ID: 127814482 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:17295261-17295783 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17295263..17295785) | | |
ID: 127814481 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:17294738-17295260 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17294740..17295262) | | |
ID: 127814480 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:17290716-17291321 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17290718..17291323) | | |
ID: 127814479 | H3K27ac hESC enhancer GRCh37_chr9:17135319-17135882 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17135321..17135884) | | |
ID: 124225054 | OCT4-NANOG hESC enhancer GRCh37_chr9:17397207-17397728 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17397209..17397730) | | |
ID: 110120694 | VISTA enhancer hs529 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17322202..17324373) | | |
ID: 107987051 | uncharacterized LOC107987051 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17547867..17555703) | | |
ID: 106480528 | RNA, 7SL, cytoplasmic 720, pseudogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17053901..17054202) | | |
ID: 100271893 | SAMM50 sorting and assembly machinery component pseudogene 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17447002..17448615, complement) | | |
ID: 100271197 | ribosomal protein L31 pseudogene 42 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17108301..17108634, complement) | RPL31_13_966 | |
ID: 54875 | centlein [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17135040..17528634) | C9orf101, C9orf39, bA340N12.1 | 611870 |