| ID: 132089609 | Neanderthal introgressed variant-containing enhancer experimental_103770 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (98018764..98018933) | | |
| ID: 132089608 | Neanderthal introgressed variant-containing enhancer experimental_103766 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (98012784..98012953) | | |
| ID: 130000804 | ATAC-STARR-seq lymphoblastoid active region 27672 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (98045477..98045626) | | |
| ID: 130000803 | ATAC-STARR-seq lymphoblastoid active region 27671 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (98037061..98037170) | | |
| ID: 130000802 | ATAC-STARR-seq lymphoblastoid active region 27670 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (97980142..97980191) | | |
| ID: 127459986 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:99057921-99058857 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (98045693..98046629) | | |
| ID: 127459985 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:99023104-99023762 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (98010876..98011534) | | |
| ID: 127459984 | H3K4me1 hESC enhancer GRCh37_chr8:99019619-99020119 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (98007391..98007891) | | |
| ID: 127459983 | H3K4me1 hESC enhancer GRCh37_chr8:98963313-98963863 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (97951085..97951635) | | |
| ID: 127459982 | H3K4me1 hESC enhancer GRCh37_chr8:98962761-98963312 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (97950533..97951084) | | |
| ID: 127459981 | H3K4me1 hESC enhancer GRCh37_chr8:98909071-98909570 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (97896843..97897342) | | |
| ID: 127459980 | H3K4me1 hESC enhancer GRCh37_chr8:98880393-98880892 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (97868165..97868664) | | |
| ID: 126860448 | BRD4-independent group 4 enhancer GRCh37_chr8:99044769-99045968 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (98032541..98033740) | | |
| ID: 124901987 | uncharacterized LOC124901987 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (97949707..97952302) | | |
| ID: 106481679 | SUMO2 pseudogene 18 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (97857849..97859003, complement) | | |
| ID: 106479876 | RNA, U6 small nuclear 703, pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (98048856..98048962) | | |
| ID: 93948 | ribosomal protein S23 pseudogene 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (97865024..97865533) | RPS23RG1, RPS23_3_930 | |
| ID: 26775 | small nucleolar RNA, H/ACA box 72 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (98042086..98042217, complement) | RNU72, U72 | |
| ID: 6156 | ribosomal protein L30 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (98041721..98045545, complement) | L30, eL30 | 180467 |
| ID: 4147 | matrilin 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (97869064..98036724) | | 602108 |