ID: 132090838 | Neanderthal introgressed variant-containing enhancer experimental_21450 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44852874..44853043) | | |
ID: 132090837 | Neanderthal introgressed variant-containing enhancer experimental_21436 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44832055..44832224) | | |
ID: 132090836 | Neanderthal introgressed variant-containing enhancer experimental_21423 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44819048..44819217) | | |
ID: 132089940 | Neanderthal introgressed variant-containing enhancer experimental_21442 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44845863..44846032) | | |
ID: 132089939 | Neanderthal introgressed variant-containing enhancer experimental_21441 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44845350..44845519) | | |
ID: 132089938 | Neanderthal introgressed variant-containing enhancer experimental_21440 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44836479..44836648) | | |
ID: 132089937 | Neanderthal introgressed variant-containing enhancer experimental_21411 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44780399..44780568) | | |
ID: 130005618 | ATAC-STARR-seq lymphoblastoid silent region 3282 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44950813..44951072) | | |
ID: 130005617 | ATAC-STARR-seq lymphoblastoid silent region 3281 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44950653..44950782) | | |
ID: 130005616 | ATAC-STARR-seq lymphoblastoid active region 4664 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44915576..44915675) | | |
ID: 130005615 | ATAC-STARR-seq lymphoblastoid active region 4663 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44862854..44862903) | | |
ID: 130005614 | ATAC-STARR-seq lymphoblastoid silent region 3279 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44727925..44728094) | | |
ID: 127820899 | H3K4me1 hESC enhancer GRCh37_chr11:44966723-44967326 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44945172..44945775) | | |
ID: 127820898 | H3K4me1 hESC enhancer GRCh37_chr11:44964865-44965513 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44943314..44943962) | | |
ID: 127820897 | H3K4me1 hESC enhancer GRCh37_chr11:44960045-44960758 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44938494..44939207) | | |
ID: 127820896 | H3K4me1 hESC enhancer GRCh37_chr11:44957874-44958474 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44936323..44936923) | | |
ID: 127820895 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:44952242-44952850 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44930691..44931299) | | |
ID: 127820894 | H3K4me1 hESC enhancer GRCh37_chr11:44944349-44944850 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44922798..44923299) | | |
ID: 127820893 | H3K4me1 hESC enhancer GRCh37_chr11:44932558-44933414 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44911007..44911863) | | |
ID: 127820892 | H3K4me1 hESC enhancer GRCh37_chr11:44914725-44915296 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44893174..44893745) | | |