| ID: 127459029 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:27587170-27587710 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27729653..27730193) | | |
| ID: 127459028 | H3K27ac hESC enhancer GRCh37_chr8:27562294-27562794 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27704777..27705277) | | |
| ID: 127459027 | H3K4me1 hESC enhancer GRCh37_chr8:27508580-27509080 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27651063..27651563) | | |
| ID: 127459026 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:27491883-27492711 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27634366..27635194) | | |
| ID: 127459025 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:27491053-27491882 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27633536..27634365) | | |
| ID: 127459024 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:27474096-27474852 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27616579..27617335) | | |
| ID: 127459023 | H3K4me1 hESC enhancer GRCh37_chr8:27473305-27473805 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27615788..27616288) | | |
| ID: 124902093 | uncharacterized LOC124902093 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27755032..27755122, complement) | | |
| ID: 124901921 | uncharacterized LOC124901921 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27689256..27694189, complement) | | |
| ID: 124901920 | uncharacterized LOC124901920 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27700970..27712745) | | |
| ID: 107986934 | uncharacterized LOC107986934 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27752860..27758089) | | |
| ID: 106481934 | RNA, U6 small nuclear 1086, pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27679836..27679935) | | |
| ID: 106481583 | RNA, U6 small nuclear 1276, pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27773645..27773748) | | |
| ID: 100500871 | microRNA 3622b [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27701673..27701767, complement) | | |
| ID: 100500858 | microRNA 3622a [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27701677..27701759) | mir-3622a | |
| ID: 157570 | establishment of sister chromatid cohesion N-acetyltransferase 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27771974..27819660) | 2410004I17Rik, EFO2, EFO2p, JHS, RBS, hEFO2 | 609353 |
| ID: 55246 | coiled-coil domain containing 25 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27733316..27772640, complement) | | 619100 |
| ID: 51435 | scavenger receptor class A member 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (27633463..27734141) | APC7, CSR, CSR1, MSLR1, MSRL1 | 602728 |