ID: 132090154 | Neanderthal introgressed variant-containing enhancer experimental_31500 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99359482..99359651) | | |
ID: 132090153 | Neanderthal introgressed variant-containing enhancer experimental_31475 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99047532..99047701) | | |
ID: 132090152 | Neanderthal introgressed variant-containing enhancer experimental_31455 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98824341..98824510) | | |
ID: 130008532 | ATAC-STARR-seq lymphoblastoid silent region 4760 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99984909..99984958) | | |
ID: 130008531 | ATAC-STARR-seq lymphoblastoid silent region 4759 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99530142..99530211) | | |
ID: 130008530 | ATAC-STARR-seq lymphoblastoid silent region 4758 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99382185..99382284) | | |
ID: 130008529 | ATAC-STARR-seq lymphoblastoid active region 6850 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99131982..99132051) | | |
ID: 130008528 | ATAC-STARR-seq lymphoblastoid active region 6849 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99131232..99131281) | | |
ID: 127824830 | H3K4me1 hESC enhancer GRCh37_chr12:100377744-100378574 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99983966..99984796) | | |
ID: 127824829 | NANOG-H3K4me1 hESC enhancer GRCh37_chr12:100117017-100117569 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99723239..99723791) | | |
ID: 127824828 | H3K27ac hESC enhancer GRCh37_chr12:100074143-100074643 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99680365..99680865) | | |
ID: 127824827 | OCT4-NANOG hESC enhancer GRCh37_chr12:100064333-100064865 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99670555..99671087) | | |
ID: 127824826 | NANOG-H3K27ac hESC enhancer GRCh37_chr12:99849451-99849950 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99455673..99456172) | | |
ID: 127824825 | NANOG-H3K27ac hESC enhancer GRCh37_chr12:99848949-99849450 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99455171..99455672) | | |
ID: 127824824 | H3K27ac hESC enhancer GRCh37_chr12:99548399-99548898 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99154621..99155120) | | |
ID: 127824823 | OCT4-NANOG hESC enhancer GRCh37_chr12:99502667-99503267 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99108889..99109489) | | |
ID: 127824822 | OCT4-NANOG hESC enhancer GRCh37_chr12:99303485-99304033 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98909707..98910255) | | |
ID: 127824821 | H3K4me1 hESC enhancer GRCh37_chr12:99288347-99288846 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98894569..98895068) | | |
ID: 127824820 | OCT4-NANOG hESC enhancer GRCh37_chr12:99254871-99255612 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98861093..98861834) | | |
ID: 127824819 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr12:99250806-99251403 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98857028..98857625) | | |