ID: 127815701 | NANOG hESC enhancer GRCh37_chr9:117955993-117956512 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (115193714..115194233) | | |
ID: 127815700 | OCT4-NANOG hESC enhancer GRCh37_chr9:117944498-117945043 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (115182219..115182764) | | |
ID: 127815699 | H3K4me1 hESC enhancer GRCh37_chr9:117895155-117895655 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (115132876..115133376) | | |
ID: 127815698 | H3K4me1 hESC enhancer GRCh37_chr9:117894654-117895154 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (115132375..115132875) | | |
ID: 127815697 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:117880715-117881534 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (115118436..115119255) | | |
ID: 126860742 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr9:117876192-117877391 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (115113913..115115112) | | |
ID: 124902257 | uncharacterized LOC124902257 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (115157394..115169734) | | |
ID: 124902255 | uncharacterized LOC124902255 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (115087391..115122544) | | |
ID: 101928748 | uncharacterized LOC101928748 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (115119539..115138409, complement) | | |
ID: 50514 | deleted in esophageal cancer 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (115141818..115402644) | CTS9, DEC1 | 604767 |
ID: 3371 | tenascin C [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (115019575..115118157, complement) | 150-225, DFNA56, GMEM, GP, HXB, JI, TN, TN-C | 187380 |