| ID: 127270589 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:158975703-158976226 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (159005913..159006436) | | |
| ID: 127270588 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:158975177-158975702 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (159005387..159005912) | | |
| ID: 127270587 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:158922455-158923423 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (158952665..158953633) | | |
| ID: 127270585 | H3K4me1 hESC enhancer GRCh37_chr1:158856217-158856716 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (158886427..158886926) | | |
| ID: 126805886 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:158984807-158986006 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (159015017..159016216) | | |
| ID: 126805885 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:158908087-158909286 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (158938297..158939496) | | |
| ID: 124904432 | uncharacterized LOC124904432 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (159012507..159014050, complement) | | |
| ID: 107181291 | pyrin domain containing 5 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (158999971..159002751, complement) | POP3 | |
| ID: 100189166 | tRNA-Arg (anticodon TCT) 4-1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (159141611..159141684, complement) | TRNAR16 | |
| ID: 100129690 | RAD1 pseudogene 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (159080940..159081693, complement) | | |
| ID: 149628 | pyrin and HIN domain family member 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (158931552..158990870) | IFIX | 612677 |
| ID: 9447 | absent in melanoma 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (159055051..159147132, complement) | PYHIN4 | 604578 |
| ID: 3428 | interferon gamma inducible protein 16 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (158999976..159055151) | IFNGIP1, PYHIN2 | 147586 |