ID: 127893502 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:45986483-45987088 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47357710..47358344) | | |
ID: 127893501 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:45983444-45984051 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47354700..47355307) | | |
ID: 127893500 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:45974595-45975341 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47345851..47346597) | | |
ID: 127893499 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:45971039-45971820 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47342295..47343076) | | |
ID: 127893498 | H3K4me1 hESC enhancer GRCh37_chr20:45968129-45968628 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47339385..47339884) | | |
ID: 127893497 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:45965286-45966124 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47336542..47337380) | | |
ID: 127893496 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:45964446-45965285 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47335702..47336541) | | |
ID: 127893495 | H3K27ac hESC enhancer GRCh37_chr20:45959988-45960488 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47331244..47331744) | | |
ID: 127893494 | H3K27ac hESC enhancer GRCh37_chr20:45957753-45958400 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47329009..47329656) | | |
ID: 127893493 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:45950739-45951656 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47321995..47322912) | | |
ID: 127893492 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:45947984-45948902 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47319240..47320158) | | |
ID: 127893491 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:45947067-45947983 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47318323..47319239) | | |
ID: 127893490 | H3K4me1 hESC enhancer GRCh37_chr20:45905089-45905589 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47276345..47276845) | | |
ID: 127893489 | H3K4me1 hESC enhancer GRCh37_chr20:45904588-45905088 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47275844..47276344) | | |
ID: 127893488 | H3K27ac hESC enhancer GRCh37_chr20:45881941-45882441 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47253197..47253697) | | |
ID: 127893487 | H3K4me1 hESC enhancer GRCh37_chr20:45863077-45863577 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47234333..47234833) | | |
ID: 127893486 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:45837467-45838090 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47208822..47209445) | | |
ID: 127893485 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:45836841-45837466 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47208196..47208821) | | |
ID: 126863042 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr20:45945484-45946683 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47316487..47318322) | | |
ID: 125387281 | Sharpr-MPRA regulatory region 15539 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47281465..47281759) | | |