ID: 132088843 | Neanderthal introgressed variant-containing enhancer experimental_58378 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3826688..3826857) | | |
ID: 132088842 | Neanderthal introgressed variant-containing enhancer experimental_58341 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3807097..3807266) | | |
ID: 132088841 | Neanderthal introgressed variant-containing enhancer experimental_58308 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3770782..3770951) | | |
ID: 129933009 | ATAC-STARR-seq lymphoblastoid active region 15238 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3662193..3662302) | | |
ID: 129933008 | ATAC-STARR-seq lymphoblastoid active region 15236 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3651551..3651830) | | |
ID: 129933007 | ATAC-STARR-seq lymphoblastoid active region 15235 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3624654..3624893) | | |
ID: 129933006 | ATAC-STARR-seq lymphoblastoid active region 15234 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3624404..3624623) | | |
ID: 129660574 | ReSE screen-validated silencer GRCh37_chr2:3917111-3917319 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3869521..3869729) | | |
ID: 129660573 | ReSE screen-validated silencer GRCh37_chr2:3707659-3707935 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3660069..3660345) | | |
ID: 129660572 | ReSE screen-validated silencer GRCh37_chr2:3669609-3669758 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3622019..3622168) | | |
ID: 127272414 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:3847621-3848162 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3800031..3800572) | | |
ID: 127272413 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:3847077-3847620 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3799487..3800030) | | |
ID: 127272412 | H3K4me1 hESC enhancer GRCh37_chr2:3828257-3828757 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3780667..3781167) | | |
ID: 127272411 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:3775588-3776177 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3727998..3728587) | | |
ID: 127272410 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:3773072-3773597 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3725482..3726007) | | |
ID: 127272409 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:3772545-3773071 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3724955..3725481) | | |
ID: 127272408 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:3699531-3700279 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3651941..3652689) | | |
ID: 127272407 | H3K4me1 hESC enhancer GRCh37_chr2:3675117-3675828 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3627527..3628238) | | |
ID: 127272406 | NANOG hESC enhancer GRCh37_chr2:3662665-3663169 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3615075..3615579) | | |
ID: 127272405 | H3K27ac hESC enhancer GRCh37_chr2:3622979-3623555 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (3575389..3575965) | | |