| ID: 130066770 | ATAC-STARR-seq lymphoblastoid silent region 13358 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42975200..42975399) | | |
| ID: 130066769 | ATAC-STARR-seq lymphoblastoid silent region 13357 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42974740..42975059) | | |
| ID: 130066768 | ATAC-STARR-seq lymphoblastoid silent region 13356 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42974220..42974609) | | |
| ID: 130066767 | ATAC-STARR-seq lymphoblastoid silent region 13355 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42973750..42973909) | | |
| ID: 129664739 | ReSE screen-validated silencer GRCh37_chr21:44500286-44500457 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43080176..43080347) | | |
| ID: 129664738 | ReSE screen-validated silencer GRCh37_chr21:44408954-44409120 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42988844..42989010) | | |
| ID: 128316769 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:44506453-44507245 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43086343..43087135) | | |
| ID: 128316768 | H3K4me1 hESC enhancer GRCh37_chr21:44489917-44490540 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43069807..43070430) | | |
| ID: 128316767 | H3K4me1 hESC enhancer GRCh37_chr21:44489293-44489916 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43069183..43069806) | | |
| ID: 128316766 | H3K27ac hESC enhancer GRCh37_chr21:44482429-44482929 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43062319..43062819) | | |
| ID: 127894842 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:44412569-44413092 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42992459..42992982) | | |
| ID: 127894841 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:44402301-44402840 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42982191..42982730) | | |
| ID: 127894840 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:44401759-44402300 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42981649..42982190) | | |
| ID: 127894839 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:44401218-44401758 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42981108..42981648) | | |
| ID: 127894838 | H3K27ac hESC enhancer GRCh37_chr21:44395471-44396197 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42975361..42976087) | | |
| ID: 127894837 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:44391589-44392348 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42971479..42972238) | | |
| ID: 127894836 | H3K27ac hESC enhancer GRCh37_chr21:44387630-44388130 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42967520..42968020) | | |
| ID: 127894835 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr21:44379675-44380524 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42959565..42960414) | | |
| ID: 127894834 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr21:44377122-44377972 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42957012..42957862) | | |
| ID: 127894833 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:44376271-44377121 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42956161..42957011) | | |