| ID: 129388644 | MPRA-validated peak475 silencer [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (178011481..178011681) | | |
| ID: 127270894 | OCT4-NANOG hESC enhancer GRCh37_chr1:177928928-177929429 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (177959793..177960294) | | |
| ID: 127270893 | H3K4me1 hESC enhancer GRCh37_chr1:177905975-177906476 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (177936840..177937341) | | |
| ID: 127270892 | OCT4-NANOG hESC enhancer GRCh37_chr1:177763543-177764294 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (177794408..177795159) | | |
| ID: 127270891 | NANOG hESC enhancer GRCh37_chr1:177624802-177625303 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (177655667..177656168) | | |
| ID: 126805932 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:177883789-177884988 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (177914654..177915853) | | |
| ID: 126805931 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:177224616-177225815 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (177255480..177256679) | | |
| ID: 111240474 | CRYZL2P-SEC16B readthrough [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (177928788..178037976, complement) | | |
| ID: 105371625 | uncharacterized LOC105371625 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (177243684..177256039, complement) | | |
| ID: 102724661 | long intergenic non-protein coding RNA 1645 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (177351586..177366458) | | |
| ID: 101928778 | long intergenic non-protein coding RNA 1741 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (177700524..177710330) | | |
| ID: 730102 | crystallin zeta like 2, pseudogene [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (178006136..178038007, complement) | | |
| ID: 89866 | SEC16 homolog B, endoplasmic reticulum export factor [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (177928788..177984284, complement) | LZTR2, PGPR-p117, RGPR, RGPR-p117, SEC16S | 612855 |
| ID: 57795 | BMP/retinoic acid inducible neural specific 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (177170958..177282422) | DBCCR1L2, FAM5B | 619359 |