| ID: 127268095 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:23830689-23831522 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23504197..23505030) | | |
| ID: 127268094 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:23829854-23830688 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23503362..23504196) | | |
| ID: 127268093 | H3K4me1 hESC enhancer GRCh37_chr1:23801333-23801832 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23474840..23475339) | | |
| ID: 127268092 | H3K4me1 hESC enhancer GRCh37_chr1:23800831-23801332 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23474338..23474839) | | |
| ID: 127268091 | NANOG hESC enhancer GRCh37_chr1:23745635-23746193 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23419142..23419700) | | |
| ID: 126805658 | BRD4-independent group 4 enhancer GRCh37_chr1:23847293-23848492 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23520801..23522000) | | |
| ID: 124903876 | uncharacterized LOC124903876 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23539883..23573700) | | |
| ID: 124903875 | uncharacterized LOC124903875 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23424866..23428983) | | |
| ID: 122056790 | Sharpr-MPRA regulatory region 12987 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23444196..23444490) | | |
| ID: 121725004 | Sharpr-MPRA regulatory region 6048 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23539837..23540131) | | |
| ID: 120893123 | Sharpr-MPRA regulatory region 9848 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23377396..23377690) | | |
| ID: 101928163 | uncharacterized LOC101928163 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23521930..23528419) | | |
| ID: 55616 | ArfGAP with SH3 domain, ankyrin repeat and PH domain 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23428563..23484631, complement) | ACAP4, CENTB6, DDEFL1, UPLC1 | 616594 |
| ID: 6920 | transcription elongation factor A3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23380909..23424748, complement) | TFIIS, TFIIS.H | 604128 |
| ID: 1870 | E2F transcription factor 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23505212..23531233, complement) | E2F-2 | 600426 |