ID: 132089735 | Neanderthal introgressed variant-containing enhancer experimental_110694 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95573600..95573769) | | |
ID: 132089734 | Neanderthal introgressed variant-containing enhancer experimental_110687 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95547373..95547542) | | |
ID: 132089733 | Neanderthal introgressed variant-containing enhancer experimental_110630 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95410157..95410326) | | |
ID: 130002133 | ATAC-STARR-seq lymphoblastoid silent region 20071 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95508202..95508521) | | |
ID: 130002132 | ATAC-STARR-seq lymphoblastoid silent region 20069 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95506602..95506841) | | |
ID: 130002131 | ATAC-STARR-seq lymphoblastoid silent region 20068 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95506112..95506171) | | |
ID: 130002130 | ATAC-STARR-seq lymphoblastoid silent region 20067 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95505892..95505951) | | |
ID: 130002129 | ATAC-STARR-seq lymphoblastoid silent region 20065 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95426698..95427087) | | |
ID: 127815366 | H3K4me1 hESC enhancer GRCh37_chr9:98363413-98363912 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95601131..95601630) | | |
ID: 127815365 | H3K4me1 hESC enhancer GRCh37_chr9:98362911-98363412 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95600629..95601130) | | |
ID: 127815364 | H3K4me1 hESC enhancer GRCh37_chr9:98327201-98327700 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95564919..95565418) | | |
ID: 127815363 | H3K4me1 hESC enhancer GRCh37_chr9:98326699-98327200 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95564417..95564918) | | |
ID: 127815362 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr9:98315131-98316095 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95552849..95553813) | | |
ID: 127815361 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr9:98314166-98315130 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95551884..95552848) | | |
ID: 127815360 | H3K27ac hESC enhancer GRCh37_chr9:98272951-98273714 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95510669..95511432) | | |
ID: 127815359 | NANOG hESC enhancer GRCh37_chr9:98271448-98271997 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95509166..95509715) | | |
ID: 127815358 | H3K27ac hESC enhancer GRCh37_chr9:98269229-98269862 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95506947..95507580) | | |
ID: 127815357 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:98256703-98257442 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95494421..95495160) | | |
ID: 127815356 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:98255961-98256702 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95493679..95494436) | | |
ID: 127815355 | H3K4me1 hESC enhancer GRCh37_chr9:98225569-98226070 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95463287..95463788) | | |