| ID: 132088821 | Neanderthal introgressed variant-containing enhancer experimental_57049 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (221259467..221259636) | | |
| ID: 129935668 | ATAC-STARR-seq lymphoblastoid silent region 12366 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (221573610..221573769) | | |
| ID: 129935667 | ATAC-STARR-seq lymphoblastoid silent region 12365 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (221573280..221573559) | | |
| ID: 129935666 | ATAC-STARR-seq lymphoblastoid silent region 12364 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (221572260..221572679) | | |
| ID: 127275849 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:222464565-222465068 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (221599845..221600348) | | |
| ID: 127275848 | NANOG hESC enhancer GRCh37_chr2:222441193-222441705 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (221576473..221576985) | | |
| ID: 127275847 | H3K4me1 hESC enhancer GRCh37_chr2:222391836-222392336 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (221527116..221527616) | | |
| ID: 127275846 | OCT4-NANOG hESC enhancer GRCh37_chr2:222333354-222333959 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (221468634..221469239) | | |
| ID: 127275845 | OCT4-NANOG hESC enhancer GRCh37_chr2:222332747-222333353 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (221468027..221468633) | | |
| ID: 127275844 | H3K27ac hESC enhancer GRCh37_chr2:222236463-222236962 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (221371743..221372242) | | |
| ID: 127275843 | NANOG hESC enhancer GRCh37_chr2:222109712-222110223 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (221244992..221245503) | | |
| ID: 127275842 | H3K4me1 hESC enhancer GRCh37_chr2:222034243-222034742 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (221169523..221170022) | | |
| ID: 127275841 | H3K4me1 hESC enhancer GRCh37_chr2:222033741-222034242 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (221169021..221169522) | | |
| ID: 127275840 | NANOG-H3K4me1 hESC enhancer GRCh37_chr2:221989613-221990137 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (221124893..221125417) | | |
| ID: 127275839 | NANOG hESC enhancer GRCh37_chr2:221646461-221647002 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (220781741..220782282) | | |
| ID: 127275838 | H3K4me1 hESC enhancer GRCh37_chr2:221614001-221614501 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (220749281..220749781) | | |
| ID: 126806527 | BRD4-independent group 4 enhancer GRCh37_chr2:222289669-222290868 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (221424949..221426148) | | |
| ID: 126806526 | MED14-independent group 3 enhancer GRCh37_chr2:221719713-221720912 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (220854993..220856192) | | |
| ID: 126806525 | MED14-independent group 3 enhancer GRCh37_chr2:221700003-221701202 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (220835283..220836482) | | |
| ID: 121725116 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr2:222381886-222383085 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (221517166..221518365) | | |