ID: 132090573 | Neanderthal introgressed variant-containing enhancer experimental_60089 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32877559..32877728) | | |
ID: 130065672 | ATAC-STARR-seq lymphoblastoid silent region 12810 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32819671..32820260) | | |
ID: 130065671 | ATAC-STARR-seq lymphoblastoid silent region 12809 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32763316..32763415) | | |
ID: 130065670 | ATAC-STARR-seq lymphoblastoid silent region 12808 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32762106..32762745) | | |
ID: 130065669 | ATAC-STARR-seq lymphoblastoid silent region 12807 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32743493..32743722) | | |
ID: 130065668 | ATAC-STARR-seq lymphoblastoid silent region 12806 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32743243..32743312) | | |
ID: 129664597 | ReSE screen-validated silencer GRCh37_chr20:31467763-31467940 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32879957..32880134) | | |
ID: 129664596 | ReSE screen-validated silencer GRCh37_chr20:31329890-31330064 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32742084..32742258) | | |
ID: 129664595 | ReSE screen-validated silencer GRCh37_chr20:31326137-31326302 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32738330..32738495) | | |
ID: 127893056 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr20:31538047-31538855 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32950241..32951049) | | |
ID: 127893055 | H3K4me1 hESC enhancer GRCh37_chr20:31505783-31506299 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32917977..32918493) | | |
ID: 127893054 | H3K4me1 hESC enhancer GRCh37_chr20:31494551-31495051 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32906745..32907245) | | |
ID: 127893053 | H3K27ac hESC enhancer GRCh37_chr20:31482477-31482988 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32894671..32895182) | | |
ID: 127893052 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:31481965-31482476 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32894159..32894670) | | |
ID: 127893051 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:31481453-31481964 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32893647..32894158) | | |
ID: 127893050 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:31480940-31481452 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32893134..32893646) | | |
ID: 127893049 | H3K27ac hESC enhancer GRCh37_chr20:31479663-31480402 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32891857..32892596) | | |
ID: 127893048 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:31474801-31475642 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32886995..32887836) | | |
ID: 127893047 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:31463559-31464528 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32875753..32876722) | | |
ID: 127893046 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:31462588-31463558 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32874782..32875752) | | |