ID: 132090687 | Neanderthal introgressed variant-containing enhancer experimental_56231 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172668509..172668678) | | |
ID: 132090686 | Neanderthal introgressed variant-containing enhancer experimental_56189 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172629073..172629242) | | |
ID: 132088801 | Neanderthal introgressed variant-containing enhancer experimental_56293 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172704850..172705019) | | |
ID: 132088800 | Neanderthal introgressed variant-containing enhancer experimental_56279 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172699825..172699994) | | |
ID: 132088799 | Neanderthal introgressed variant-containing enhancer experimental_56260 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172693304..172693473) | | |
ID: 132088798 | Neanderthal introgressed variant-containing enhancer experimental_56221 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172655599..172655768) | | |
ID: 132088797 | Neanderthal introgressed variant-containing enhancer experimental_56072 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172502147..172502316) | | |
ID: 132088796 | Neanderthal introgressed variant-containing enhancer experimental_56026 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172466263..172466432) | | |
ID: 132088795 | Neanderthal introgressed variant-containing enhancer experimental_55951 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172381681..172381850) | | |
ID: 129935114 | ATAC-STARR-seq lymphoblastoid silent region 12111 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172555762..172556491) | | |
ID: 129935113 | ATAC-STARR-seq lymphoblastoid active region 16763 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172555432..172555581) | | |
ID: 129935112 | ATAC-STARR-seq lymphoblastoid silent region 12110 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172427534..172427613) | | |
ID: 129660854 | ReSE screen-validated silencer GRCh37_chr2:173456666-173456873 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172591938..172592145) | | |
ID: 127275259 | H3K27ac hESC enhancer GRCh37_chr2:173591267-173591767 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172726539..172727039) | | |
ID: 127275258 | H3K27ac hESC enhancer GRCh37_chr2:173590766-173591266 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172726038..172726538) | | |
ID: 127275257 | H3K4me1 hESC enhancer GRCh37_chr2:173577807-173578364 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172713079..172713636) | | |
ID: 127275256 | NANOG-H3K27ac hESC enhancer GRCh37_chr2:173414302-173415043 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172549574..172550315) | | |
ID: 127275255 | NANOG-H3K27ac hESC enhancer GRCh37_chr2:173413559-173414301 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172548831..172549573) | | |
ID: 127275254 | H3K27ac hESC enhancer GRCh37_chr2:173399678-173400178 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172534950..172535450) | | |
ID: 127275253 | H3K27ac hESC enhancer GRCh37_chr2:173318135-173318864 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172453366..172454136) | | |