ID: 127402177 | H3K4me1 hESC enhancer GRCh37_chr5:533845-534364 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (533730..534249) | | |
ID: 127402176 | H3K4me1 hESC enhancer GRCh37_chr5:526131-526763 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (526016..526648) | | |
ID: 127402175 | H3K4me1 hESC enhancer GRCh37_chr5:515297-515797 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (515182..515682) | | |
ID: 127402174 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:496057-496580 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (495942..496465) | | |
ID: 127402173 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:475243-475883 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (475128..475768) | | |
ID: 127402172 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:472675-473315 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (472560..473943) | | |
ID: 127402171 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:472032-472674 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (471917..472573) | | |
ID: 126807282 | BRD4-independent group 4 enhancer GRCh37_chr5:458642-459841 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (458527..459726) | | |
ID: 124900930 | uncharacterized LOC124900930 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (446821..447392) | | |
ID: 107986395 | uncharacterized LOC107986395 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (524658..527455) | | |
ID: 100616381 | microRNA 4456 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (535840..535882, complement) | | |
ID: 100288152 | SLC9A3 antisense RNA 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (473236..480892) | UC011CLY.2 | |
ID: 116349 | EXOC3 antisense RNA 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (441835..443160, complement) | C5orf55 | |
ID: 25845 | SLC9A3 3' UTR overlapping transcript 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (470510..472965, complement) | PP7080 | |
ID: 11336 | exocyst complex component 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (443176..467290) | SEC6, SEC6L1, Sec6p | 608186 |
ID: 6550 | solute carrier family 9 member A3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (470456..524449, complement) | DIAR8, NHE-3, NHE3 | 182307 |