| ID: 127270956 | H3K4me1 hESC enhancer GRCh37_chr1:181452885-181453408 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (181483749..181484272) | | |
| ID: 127270955 | H3K4me1 hESC enhancer GRCh37_chr1:181452360-181452884 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (181483224..181483748) | | |
| ID: 127270954 | H3K4me1 hESC enhancer GRCh37_chr1:181450844-181451376 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (181481708..181482240) | | |
| ID: 127270953 | H3K4me1 hESC enhancer GRCh37_chr1:181287535-181288165 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (181318399..181319029) | | |
| ID: 127270952 | H3K4me1 hESC enhancer GRCh37_chr1:181277357-181277857 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (181308221..181308721) | | |
| ID: 126805943 | MED14-independent group 3 enhancer GRCh37_chr1:181737037-181738236 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (181767901..181769100) | | |
| ID: 112577519 | Sharpr-MPRA regulatory region 5358 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (181855454..181855748) | | |
| ID: 107985454 | uncharacterized LOC107985454 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (181309213..181312328) | | |
| ID: 107985232 | uncharacterized LOC107985232 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (181419741..181432389) | | |
| ID: 106480904 | RN7SK pseudogene 229 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (181839539..181839774, complement) | | |
| ID: 106480436 | RNA, 5S ribosomal pseudogene 70 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (181771566..181771644) | RN5S70 | |
| ID: 777 | calcium voltage-gated channel subunit alpha1 E [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (181317699..181808084) | BII, CACH6, CACNL1A6, Cav2.3, DEE69, EIEE69, gm139 | 601013 |