| ID: 127459144 | NANOG hESC enhancer GRCh37_chr8:36807536-36808072 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (36950018..36950554) | | |
| ID: 126860355 | MED14-independent group 3 enhancer GRCh37_chr8:36780820-36782019 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (36923302..36924501) | | |
| ID: 124906685 | uncharacterized LOC124906685 [Homo sapiens (human)] | | | |
| ID: 105379376 | uncharacterized LOC105379376 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (36963696..36982005, complement) | | |
| ID: 105379375 | uncharacterized LOC105379375 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (36881916..36925207, complement) | | |
| ID: 100873517 | RNA, 5S ribosomal pseudogene 264 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (36764445..36764551) | RN5S264 | |
| ID: 100270966 | ribosomal protein L26 pseudogene 25 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (36987930..36988457, complement) | RPL26_6_894 | |
| ID: 359783 | mitochondrial ribosomal protein S7 pseudogene 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (36795263..36795967, complement) | | |
| ID: 157855 | potassium calcium-activated channel subfamily U member 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (36784374..36936125) | KCNMC1, KCa5, KCa5.1, Kcnma3, SPGF79, Slo3 | 615215 |
| ID: 59347 | TPT1 pseudogene 8 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (36888370..36889530) | FKSG2 | |