| ID: 132089591 | Neanderthal introgressed variant-containing enhancer experimental_102829 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22246237..22246406) | | |
| ID: 132089590 | Neanderthal introgressed variant-containing enhancer experimental_102823 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22230634..22230803) | | |
| ID: 129999976 | ATAC-STARR-seq lymphoblastoid silent region 18982 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22164628..22165667) | | |
| ID: 127458875 | H3K27ac hESC enhancer GRCh37_chr8:22102421-22103088 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22244908..22245602) | | |
| ID: 127458874 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:22089242-22089989 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22231729..22232476) | | |
| ID: 127458873 | H3K4me1 hESC enhancer GRCh37_chr8:22081363-22081865 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22223850..22224352) | | |
| ID: 127458872 | H3K4me1 hESC enhancer GRCh37_chr8:22077527-22078227 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22220014..22220714) | | |
| ID: 127458871 | H3K4me1 hESC enhancer GRCh37_chr8:22071895-22072757 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22214382..22215244) | | |
| ID: 127458870 | H3K4me1 hESC enhancer GRCh37_chr8:22069059-22069750 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22211546..22212237) | | |
| ID: 127458869 | H3K4me1 hESC enhancer GRCh37_chr8:22068368-22069058 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22210855..22211545) | | |
| ID: 127458868 | H3K4me1 hESC enhancer GRCh37_chr8:22067676-22068367 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22210163..22210854) | | |
| ID: 127458867 | H3K4me1 hESC enhancer GRCh37_chr8:22054519-22055286 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22197006..22197773) | | |
| ID: 127458866 | H3K4me1 hESC enhancer GRCh37_chr8:22046165-22046665 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22188652..22189152) | | |
| ID: 127458865 | H3K27ac hESC enhancer GRCh37_chr8:22031123-22031622 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22173610..22174109) | | |
| ID: 126860324 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr8:22084886-22086085 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22227114..22228572) | | |
| ID: 126860323 | BRD4-independent group 4 enhancer GRCh37_chr8:22048316-22049515 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22190803..22192002) | | |
| ID: 124901904 | uncharacterized LOC124901904 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22187776..22191595, complement) | | |
| ID: 124153118 | Sharpr-MPRA regulatory region 11422 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22237336..22237630) | | |
| ID: 113788269 | BRD4-independent group 4 enhancer GRCh37_chr8:22052064-22053263 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22194376..22195750) | | |
| ID: 100507071 | PIWIL2 divergent transcript [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22254576..22275162, complement) | | |