ID: 132090559 | Neanderthal introgressed variant-containing enhancer experimental_51899 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56132356..56132525) | | |
ID: 132090558 | Neanderthal introgressed variant-containing enhancer experimental_51865 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56127391..56127560) | | |
ID: 132090557 | Neanderthal introgressed variant-containing enhancer experimental_51805 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56090920..56091089) | | |
ID: 130065152 | ATAC-STARR-seq lymphoblastoid active region 15115 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56141110..56141249) | | |
ID: 130065151 | ATAC-STARR-seq lymphoblastoid active region 15114 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56140750..56141079) | | |
ID: 130065150 | ATAC-STARR-seq lymphoblastoid active region 15113 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56113366..56113475) | | |
ID: 130065149 | ATAC-STARR-seq lymphoblastoid active region 15112 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56110639..56110708) | | |
ID: 130065148 | ATAC-STARR-seq lymphoblastoid silent region 11063 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56081458..56081517) | | |
ID: 130065147 | ATAC-STARR-seq lymphoblastoid active region 15111 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56080978..56081127) | | |
ID: 130065146 | ATAC-STARR-seq lymphoblastoid silent region 11062 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56080628..56080687) | | |
ID: 127892304 | H3K4me1 hESC enhancer GRCh37_chr19:56640701-56641201 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56129332..56129832) | | |
ID: 127892303 | H3K4me1 hESC enhancer GRCh37_chr19:56640200-56640700 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56128794..56129331) | | |
ID: 127892302 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:56632431-56633146 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56121062..56121791) | | |
ID: 127892301 | H3K4me1 hESC enhancer GRCh37_chr19:56628849-56629564 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56117480..56118195) | | |
ID: 127892300 | H3K4me1 hESC enhancer GRCh37_chr19:56626767-56627443 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56115398..56116074) | | |
ID: 127892299 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:56622697-56623374 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56111328..56112005) | | |
ID: 127892298 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:56597714-56598313 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56086348..56086947) | | |
ID: 127892297 | H3K4me1 hESC enhancer GRCh37_chr19:56596879-56597378 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56085513..56086012) | | |
ID: 127892296 | H3K4me1 hESC enhancer GRCh37_chr19:56596377-56596878 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56085011..56085512) | | |
ID: 126862936 | MED14-independent group 3 enhancer GRCh37_chr19:56602588-56603787 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (56091219..56092435) | | |