ID: 132089053 | Neanderthal introgressed variant-containing enhancer experimental_74908 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (153831698..153831867) | | |
ID: 132089052 | Neanderthal introgressed variant-containing enhancer experimental_74906 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (153828288..153828457) | | |
ID: 132089051 | Neanderthal introgressed variant-containing enhancer experimental_74905 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (153827402..153827571) | | |
ID: 132089050 | Neanderthal introgressed variant-containing enhancer experimental_74898 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (153822891..153823060) | | |
ID: 132089049 | Neanderthal introgressed variant-containing enhancer experimental_74882 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (153806331..153806500) | | |
ID: 132089048 | Neanderthal introgressed variant-containing enhancer experimental_74875 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (153804450..153804619) | | |
ID: 132089047 | Neanderthal introgressed variant-containing enhancer experimental_74859 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (153792924..153793093) | | |
ID: 132089046 | Neanderthal introgressed variant-containing enhancer experimental_74856/74857 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (153790976..153791145) | | |
ID: 132089045 | Neanderthal introgressed variant-containing enhancer experimental_74848 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (153771318..153771487) | | |
ID: 132089044 | Neanderthal introgressed variant-containing enhancer experimental_74840 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (153719886..153720055) | | |
ID: 129993289 | ATAC-STARR-seq lymphoblastoid active region 22073 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (154368327..154368396) | | |
ID: 129993288 | ATAC-STARR-seq lymphoblastoid active region 22072 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (153916391..153916510) | | |
ID: 129993287 | ATAC-STARR-seq lymphoblastoid silent region 15767 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (153684458..153684547) | | |
ID: 129661350 | ReSE screen-validated silencer GRCh37_chr4:154871827-154872023 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (153950675..153950871) | | |
ID: 129661349 | ReSE screen-validated silencer GRCh37_chr4:154802179-154802342 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (153881027..153881190) | | |
ID: 129389243 | MPRA-validated peak5134 silencer [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (154189443..154189643) | | |
ID: 127401777 | H3K4me1 hESC enhancer GRCh37_chr4:154945006-154945526 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (154023854..154024374) | | |
ID: 127401776 | H3K4me1 hESC enhancer GRCh37_chr4:154944484-154945005 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (154023332..154023853) | | |
ID: 127401775 | H3K27ac hESC enhancer GRCh37_chr4:154855107-154855606 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (153933955..153934454) | | |
ID: 127401774 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:154711165-154711866 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (153790013..153790714) | | |