| ID: 132089523 | Neanderthal introgressed variant-containing enhancer experimental_98226 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (21155648..21155817) | | |
| ID: 129998036 | ATAC-STARR-seq lymphoblastoid silent region 17994 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20798348..20798477) | | |
| ID: 129998035 | ATAC-STARR-seq lymphoblastoid silent region 17993 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20798028..20798257) | | |
| ID: 129998034 | ATAC-STARR-seq lymphoblastoid silent region 17992 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20797918..20797977) | | |
| ID: 127408595 | OCT4-NANOG hESC enhancer GRCh37_chr7:21069658-21070388 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (21030039..21030769) | | |
| ID: 127408594 | H3K4me1 hESC enhancer GRCh37_chr7:20874484-20874984 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20834865..20835365) | | |
| ID: 127408593 | NANOG hESC enhancer GRCh37_chr7:20855921-20856533 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20816302..20816914) | | |
| ID: 127408592 | OCT4-NANOG hESC enhancer GRCh37_chr7:20835446-20836154 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20795827..20796535) | | |
| ID: 127408591 | H3K27ac hESC enhancer GRCh37_chr7:20822883-20823543 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20783264..20783924) | | |
| ID: 127408590 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr7:20816339-20816919 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20776719..20777299) | | |
| ID: 127408589 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr7:20815756-20816338 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20776136..20776718) | | |
| ID: 127408588 | NANOG hESC enhancer GRCh37_chr7:20693236-20693793 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20653613..20654170) | | |
| ID: 126859960 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr7:21050446-21051645 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (21010827..21012026) | | |
| ID: 126859959 | BRD4-independent group 4 enhancer GRCh37_chr7:20866537-20867736 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20826918..20828117) | | |
| ID: 126859958 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr7:20681108-20682307 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20641485..20642684) | | |
| ID: 110121034 | VISTA enhancer hs1226 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (21041182..21042467) | | |
| ID: 110121006 | VISTA enhancer hs1148 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20979932..20981581) | | |
| ID: 110120964 | VISTA enhancer hs1019 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20799224..20800776) | | |
| ID: 110120961 | VISTA enhancer hs1007 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20958049..20959483) | | |
| ID: 110120786 | VISTA enhancer hs844 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20793009..20794283) | | |