| ID: 127267714 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:17053781-17054392 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16727286..16727897) | | |
| ID: 127267713 | H3K4me1 hESC enhancer GRCh37_chr1:17045407-17045959 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16718912..16719464) | | |
| ID: 127267712 | H3K4me1 hESC enhancer GRCh37_chr1:17044853-17045406 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16718358..16718911) | | |
| ID: 127267711 | H3K4me1 hESC enhancer GRCh37_chr1:17043745-17044298 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16717250..16717803) | | |
| ID: 127267710 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:17034628-17035166 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16708133..16708671) | | |
| ID: 127267709 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:17034088-17034627 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16707593..16708132) | | |
| ID: 127267708 | H3K4me1 hESC enhancer GRCh37_chr1:17027493-17028178 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16700998..16701683) | | |
| ID: 127267707 | NANOG-H3K4me1 hESC enhancer GRCh37_chr1:17021274-17022100 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16694779..16695605) | | |
| ID: 127267706 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:17020446-17021273 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16693951..16694778) | | |
| ID: 127267705 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:17019619-17020445 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16693124..16693950) | | |
| ID: 124903858 | uncharacterized LOC124903858 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16699997..16705455) | | |
| ID: 107985759 | tRNA-Gly (CCC) 4-1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16678271..16678341, complement) | TRNAG36, TRNAV35P | |
| ID: 100189500 | tRNA-Val (CAC) 13-1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16725566..16725638) | TRNAV36P | |
| ID: 100189045 | tRNA-Gly (CCC) 5-1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16727285..16727355) | TRNAG10 | |
| ID: 284729 | espin pseudogene [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16691218..16720157, complement) | dJ1182A14.1 | |
| ID: 280661 | EIF1AX pseudogene 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16683091..16686249, complement) | EIF1AP1 | |