ID: 127397972 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr3:71546600-71547538 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71497449..71498387) | | |
ID: 127397971 | H3K4me1 hESC enhancer GRCh37_chr3:71463501-71464005 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71414350..71414854) | | |
ID: 127397970 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr3:71354949-71355604 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71305798..71306453) | | |
ID: 127397969 | H3K4me1 hESC enhancer GRCh37_chr3:71275618-71276118 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71226467..71226967) | | |
ID: 127397968 | NANOG hESC enhancer GRCh37_chr3:71259322-71259867 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71210171..71210716) | | |
ID: 127397967 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:71205831-71206536 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71156680..71157385) | | |
ID: 127397966 | H3K27ac hESC enhancer GRCh37_chr3:71193639-71194138 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71144488..71144987) | | |
ID: 127397965 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr3:71178876-71179618 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71129725..71130467) | | |
ID: 127397964 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr3:71128185-71128767 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71079034..71079616) | | |
ID: 127397963 | H3K27ac hESC enhancer GRCh37_chr3:71114251-71114751 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71065100..71065600) | | |
ID: 127397962 | OCT4-NANOG hESC enhancer GRCh37_chr3:71012492-71013094 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (70963341..70963943) | | |
ID: 127397961 | OCT4 hESC enhancer GRCh37_chr3:70976354-70976889 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (70927203..70927738) | | |
ID: 127397960 | H3K27ac hESC enhancer GRCh37_chr3:70926235-70926734 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (70877084..70877583) | | |
ID: 126806715 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr3:71552767-71553966 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71503616..71504815) | | |
ID: 126806714 | BRD4-independent group 4 enhancer GRCh37_chr3:71025197-71026396 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (70976046..70977245) | | |
ID: 126568846 | FOXP1 divergent transcript [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71584943..71587409) | | |
ID: 124906248 | uncharacterized LOC124906248 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71337930..71350976) | | |
ID: 124906247 | uncharacterized LOC124906247 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71073220..71088715) | | |
ID: 123002305 | Sharpr-MPRA regulatory region 15380 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71510558..71510852) | | |
ID: 123002304 | Sharpr-MPRA regulatory region 10822 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71453378..71453672) | | |