ID: 132089505 | Neanderthal introgressed variant-containing enhancer experimental_100118 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (80753624..80753793) | | |
ID: 129998723 | ATAC-STARR-seq lymphoblastoid silent region 18334 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (80919188..80919317) | | |
ID: 129998722 | ATAC-STARR-seq lymphoblastoid active region 26210 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (80918571..80918640) | | |
ID: 129662033 | ReSE screen-validated silencer GRCh37_chr7:80627598-80627796 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (80998282..80998480) | | |
ID: 127456888 | H3K4me1 hESC enhancer GRCh37_chr7:80924025-80924526 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81294709..81295210) | | |
ID: 127456887 | OCT4-NANOG hESC enhancer GRCh37_chr7:80809759-80810307 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81180443..81180991) | | |
ID: 127456886 | NANOG hESC enhancer GRCh37_chr7:80642207-80642710 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81012891..81013394) | | |
ID: 127456885 | OCT4-NANOG hESC enhancer GRCh37_chr7:80393335-80394071 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (80764019..80764755) | | |
ID: 127456884 | NANOG hESC enhancer GRCh37_chr7:80162485-80162986 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (80533169..80533670) | | |
ID: 127456883 | H3K27ac hESC enhancer GRCh37_chr7:80157849-80158348 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (80528533..80529032) | | |
ID: 126860084 | BRD4-independent group 4 enhancer GRCh37_chr7:80983381-80984580 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81354065..81355264) | | |
ID: 126860083 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr7:80703763-80704962 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81074447..81075646) | | |
ID: 126860082 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr7:80512613-80513812 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (80883297..80884496) | | |
ID: 126860081 | MED14-independent group 3 enhancer GRCh37_chr7:80163190-80164389 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (80533874..80535073) | | |
ID: 124901686 | uncharacterized LOC124901686 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (80792105..80797783, complement) | | |
ID: 124901685 | uncharacterized LOC124901685 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (80524847..80546667) | | |
ID: 123956173 | Sharpr-MPRA regulatory region 7331 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (80722853..80723147) | | |
ID: 111413046 | HNF1 motif-containing MPRA enhancer 195 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81155928..81156072) | | |
ID: 100421455 | eukaryotic translation initiation factor 4E pseudogene 4 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81463036..81463613, complement) | | |
ID: 100420647 | voltage dependent anion channel 3 pseudogene [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81191361..81192009) | | |