| ID: 127460246 | H3K4me1 hESC enhancer GRCh37_chr8:124186535-124187034 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (123174295..123174794) | | |
| ID: 126860492 | BRD4-independent group 4 enhancer GRCh37_chr8:124160865-124162064 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (123148625..123149824) | | |
| ID: 124902013 | uncharacterized LOC124902013 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (123002560..123030756) | | |
| ID: 124188217 | Sharpr-MPRA regulatory region 15016 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (123083009..123083303) | | |
| ID: 113788253 | Sharpr-MPRA regulatory region 4427 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (123166222..123167951) | | |
| ID: 100419979 | high mobility group box 1 pseudogene 19 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (123123110..123123684) | | |
| ID: 100379299 | RNY4 pseudogene 5 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (123044717..123044811) | | |
| ID: 100189201 | tRNA-Met (anticodon CAT) 1-1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (123157230..123157302, complement) | TRNAM11 | |
| ID: 93594 | TBC1 domain family member 31 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (123072707..123165173) | Gm85, WDR67 | |
| ID: 79139 | derlin 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (123013170..123042302, complement) | DER-1, DER1, derlin-1 | 608813 |