| ID: 127825771 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:132284875-132285724 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131800330..131801179) | | |
| ID: 127825770 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:132281963-132282784 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131797418..131798239) | | |
| ID: 127825769 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:132280316-132281138 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131795771..131796593) | | |
| ID: 127825768 | H3K4me1 hESC enhancer GRCh37_chr12:132271907-132272407 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131787362..131787862) | | |
| ID: 127825767 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:132258607-132259231 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131774062..131774686) | | |
| ID: 127825766 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:132257981-132258606 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131773436..131774061) | | |
| ID: 127825765 | H3K27ac hESC enhancer GRCh37_chr12:132217158-132217826 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131732613..131733281) | | |
| ID: 127825764 | H3K27ac hESC enhancer GRCh37_chr12:132216488-132217157 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131731943..131732612) | | |
| ID: 127825763 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:132213273-132213837 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131728728..131729292) | | |
| ID: 127825762 | H3K4me1 hESC enhancer GRCh37_chr12:132156613-132157112 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131672068..131672567) | | |
| ID: 126861694 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr12:132269252-132270451 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131784707..131785906) | | |
| ID: 126861693 | BRD4-independent group 4 enhancer GRCh37_chr12:132221080-132222279 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131736535..131737734) | | |
| ID: 126861692 | MED14-independent group 3 enhancer GRCh37_chr12:132204952-132206151 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131720407..131721606) | | |
| ID: 124903057 | uncharacterized LOC124903057 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131670987..131673398) | | |
| ID: 106480014 | RNA, U6 small nuclear 1017, pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131815263..131815368, complement) | | |
| ID: 105370087 | uncharacterized LOC105370087 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131677708..131692697) | | |
| ID: 100873634 | RNA, 5S ribosomal pseudogene 378 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131801315..131801434, complement) | RN5S378 | |
| ID: 6433 | splicing factor SWAP [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (131711090..131799738) | SFRS8, SWAP | 601945 |