| ID: 130066850 | ATAC-STARR-seq lymphoblastoid silent region 13401 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45287822..45288351) | | |
| ID: 130066849 | ATAC-STARR-seq lymphoblastoid active region 18586 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45125450..45125629) | | |
| ID: 130066848 | ATAC-STARR-seq lymphoblastoid silent region 13400 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45113778..45113827) | | |
| ID: 130066847 | ATAC-STARR-seq lymphoblastoid silent region 13399 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45074334..45074533) | | |
| ID: 130066846 | ATAC-STARR-seq lymphoblastoid silent region 13398 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45074224..45074313) | | |
| ID: 127895031 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:46714121-46714627 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45294206..45294712) | | |
| ID: 127895030 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:46712089-46712596 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45292174..45292681) | | |
| ID: 127895029 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:46711580-46712088 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45291665..45292173) | | |
| ID: 127895028 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:46708421-46709151 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45288506..45289236) | | |
| ID: 127895027 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:46675963-46676514 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45256048..45256599) | | |
| ID: 127895026 | H3K4me1 hESC enhancer GRCh37_chr21:46640206-46640772 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45220291..45220857) | | |
| ID: 127895025 | H3K4me1 hESC enhancer GRCh37_chr21:46626875-46627374 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45206960..45207459) | | |
| ID: 127895024 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:46622742-46623359 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45202827..45203444) | | |
| ID: 127895023 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:46580749-46581394 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45160834..45161479) | | |
| ID: 127895022 | H3K4me1 hESC enhancer GRCh37_chr21:46571268-46572124 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45151353..45152209) | | |
| ID: 127895021 | H3K4me1 hESC enhancer GRCh37_chr21:46569001-46569596 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45149086..45149681) | | |
| ID: 127895020 | H3K4me1 hESC enhancer GRCh37_chr21:46553929-46554429 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45134014..45134514) | | |
| ID: 127895019 | H3K4me1 hESC enhancer GRCh37_chr21:46553428-46553928 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45133513..45134013) | | |
| ID: 127895018 | H3K4me1 hESC enhancer GRCh37_chr21:46513297-46513797 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45093382..45093882) | | |
| ID: 126653401 | MED14-independent group 3 enhancer GRCh37_chr21:46699476-46700675 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45279561..45280760) | | |