| ID: 130000629 | ATAC-STARR-seq lymphoblastoid silent region 19306 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (77118833..77118892) | | |
| ID: 130000628 | ATAC-STARR-seq lymphoblastoid silent region 19305 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (76811450..76811509) | | |
| ID: 129390013 | MPRA-validated peak7079 silencer [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (77067440..77067640) | | |
| ID: 127459801 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:78000945-78001521 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (77088709..77089285) | | |
| ID: 127459800 | OCT4-NANOG hESC enhancer GRCh37_chr8:77676670-77677613 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (76764434..76765377) | | |
| ID: 113788293 | Sharpr-MPRA regulatory region 11833 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (77000073..77000367) | | |
| ID: 110121186 | VISTA enhancer hs1681 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (76839317..76842107) | | |
| ID: 110121054 | VISTA enhancer hs1318 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (76685772..76688410) | | |
| ID: 110120766 | VISTA enhancer hs774 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (76778447..76779543) | | |
| ID: 110120756 | VISTA enhancer hs742 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (77130335..77131965) | | |
| ID: 105375909 | uncharacterized LOC105375909 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (77399072..77421357) | | |
| ID: 100874456 | HIG1 hypoxia inducible domain family member 1A pseudogene 18 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (77013556..77014088, complement) | | |
| ID: 100422921 | microRNA 3149 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (76966768..76966850, complement) | | |
| ID: 100192378 | ZFHX4 antisense RNA 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (76610879..76683275, complement) | | |
| ID: 79776 | zinc finger homeobox 4 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (76681247..76867281) | ZFH4, ZHF4 | 606940 |
| ID: 5828 | peroxisomal biogenesis factor 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (76980258..77001044, complement) | PAF1, PBD5A, PBD5B, PMP3, PMP35, PXMP3, RNF72, ZWS3 | 170993 |