| ID: 132090783 | Neanderthal introgressed variant-containing enhancer experimental_101206 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13558670..13558839) | | |
| ID: 129999925 | ATAC-STARR-seq lymphoblastoid silent region 18957 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13133449..13133518) | | |
| ID: 129999924 | ATAC-STARR-seq lymphoblastoid silent region 18956 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13133189..13133418) | | |
| ID: 129662237 | ReSE screen-validated silencer GRCh37_chr8:12957644-12958023 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13100135..13100514) | | |
| ID: 127458754 | H3K4me1 hESC enhancer GRCh37_chr8:12982671-12983171 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13125162..13125662) | | |
| ID: 127458753 | H3K4me1 hESC enhancer GRCh37_chr8:12982170-12982670 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13124661..13125161) | | |
| ID: 127458752 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:12980809-12981441 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13123300..13123932) | | |
| ID: 127458751 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:12980176-12980808 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13122667..13123299) | | |
| ID: 127458750 | H3K27ac hESC enhancer GRCh37_chr8:12965381-12965880 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13107872..13108371) | | |
| ID: 127458749 | H3K4me1 hESC enhancer GRCh37_chr8:12962666-12963312 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13105157..13105803) | | |
| ID: 127458748 | H3K4me1 hESC enhancer GRCh37_chr8:12915937-12916437 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13058428..13058928) | | |
| ID: 126860306 | BRD4-independent group 4 enhancer GRCh37_chr8:13223844-13225043 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13366335..13367534) | | |
| ID: 126860305 | MED14-independent group 3 enhancer GRCh37_chr8:12947375-12948574 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13089866..13091065) | | |
| ID: 124902103 | uncharacterized LOC124902103 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13046580..13046653, complement) | | |
| ID: 124901890 | uncharacterized LOC124901890 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13462639..13478575) | | |
| ID: 106481447 | RNA, U6 small nuclear 842, pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13044350..13044455) | | |
| ID: 102725080 | uncharacterized LOC102725080 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13629690..13632576) | | |
| ID: 101930149 | uncharacterized LOC101930149 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13338338..13357485) | | |
| ID: 100873509 | RNA, 5S ribosomal pseudogene 255 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13536029..13536135) | RN5S255 | |
| ID: 100873195 | MT-ND4 pseudogene 7 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (13353397..13353608, complement) | | |