ID: 132090785 | Neanderthal introgressed variant-containing enhancer experimental_102863 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22318572..22318741) | | |
ID: 132090784 | Neanderthal introgressed variant-containing enhancer experimental_102832 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22261420..22261589) | | |
ID: 132089595 | Neanderthal introgressed variant-containing enhancer experimental_102873 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22339514..22339683) | | |
ID: 132089594 | Neanderthal introgressed variant-containing enhancer experimental_102872 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22338949..22339118) | | |
ID: 132089593 | Neanderthal introgressed variant-containing enhancer experimental_102848 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22291703..22291872) | | |
ID: 132089592 | Neanderthal introgressed variant-containing enhancer experimental_102836 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22270460..22270629) | | |
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: 129999978 | ATAC-STARR-seq lymphoblastoid active region 27078 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22367913..22368162) | | |
ID: 129999977 | ATAC-STARR-seq lymphoblastoid silent region 18984 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22366923..22367592) | | |
ID: 129662251 | ReSE screen-validated silencer GRCh37_chr8:22226031-22226209 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22368518..22368696) | | |
ID: 127458878 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:22241071-22241684 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22383558..22384171) | | |
ID: 127458877 | H3K4me1 hESC enhancer GRCh37_chr8:22223390-22223890 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22365877..22366377) | | |
ID: 127458876 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:22133109-22133754 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22275596..22276241) | | |
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: 126860324 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr8:22084886-22086085 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22227114..22228572) | | |
ID: 124153119 | Sharpr-MPRA regulatory region 10265 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22292036..22292330) | | |