ID: 127272959 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:27665383-27665925 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27442516..27443058) | | |
ID: 127272958 | H3K4me1 hESC enhancer GRCh37_chr2:27618171-27618672 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27395304..27395805) | | |
ID: 126806173 | BRD4-independent group 4 enhancer GRCh37_chr2:27676057-27677256 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27453190..27454389) | | |
ID: 200634 | keratinocyte associated protein 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27442381..27446481) | KCP3 | 619261 |
ID: 29959 | nuclear receptor binding protein 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27427790..27442259) | BCON3, MADM, MUDPNP, NRBP | 606010 |
ID: 26160 | intraflagellar transport 172 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27444377..27489743, complement) | BBS20, NPHP17, RP71, SLB, SRTD10, osm-1, wim | 607386 |
ID: 5496 | protein phosphatase, Mg2+/Mn2+ dependent 1G [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27381199..27409591, complement) | PP2CG, PP2CGAMMA, PPP2CG | 605119 |
ID: 2498 | ferritin heavy chain 1 pseudogene 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27392623..27393576, complement) | FTHL3, FTHL3P | |