ID: 127825629 | NANOG hESC enhancer GRCh37_chr12:125920548-125921070 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125436002..125436524) | | |
ID: 127825628 | H3K27ac hESC enhancer GRCh37_chr12:125861407-125861906 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125376861..125377360) | | |
ID: 127825627 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:125814395-125815120 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125329849..125330574) | | |
ID: 127825626 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:125813668-125814394 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125329122..125329848) | | |
ID: 127825625 | H3K4me1 hESC enhancer GRCh37_chr12:125798555-125799056 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125314009..125314510) | | |
ID: 127825624 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:125765450-125766312 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125280904..125281766) | | |
ID: 127825623 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:125764586-125765449 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125280040..125280903) | | |
ID: 127825622 | H3K4me1 hESC enhancer GRCh37_chr12:125730381-125730881 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125245835..125246335) | | |
ID: 127825621 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:125692947-125693686 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125208401..125209140) | | |
ID: 127825620 | H3K4me1 hESC enhancer GRCh37_chr12:125678461-125678992 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125193915..125194446) | | |
ID: 127825619 | H3K4me1 hESC enhancer GRCh37_chr12:125670133-125670666 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125185587..125186120) | | |
ID: 127825618 | H3K4me1 hESC enhancer GRCh37_chr12:125644140-125644640 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125159594..125160094) | | |
ID: 126861673 | BRD4-independent group 4 enhancer GRCh37_chr12:126022594-126023793 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125538048..125539247) | | |
ID: 124903047 | uncharacterized LOC124903047 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125858878..125861629, complement) | | |
ID: 113939934 | Sharpr-MPRA regulatory region 9406 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125518163..125518457) | | |
ID: 107984445 | uncharacterized LOC107984445 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125284111..125290400) | | |
ID: 105370055 | uncharacterized LOC105370055 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125704501..125707950) | | |
ID: 105370054 | uncharacterized LOC105370054 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125272896..125280816, complement) | | |
ID: 105370053 | uncharacterized LOC105370053 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125151338..125161019) | | |
ID: 100419701 | CTAGE family member 9 pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (125900318..125901485, complement) | | |