ID: 132089103 | Neanderthal introgressed variant-containing enhancer experimental_76710 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182803811..182803980) | | |
ID: 132089102 | Neanderthal introgressed variant-containing enhancer experimental_76678 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182465864..182466033) | | |
ID: 129993425 | ATAC-STARR-seq lymphoblastoid silent region 15825 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182917018..182917727) | | |
ID: 129993424 | ATAC-STARR-seq lymphoblastoid active region 22177 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182825925..182826104) | | |
ID: 129993423 | ATAC-STARR-seq lymphoblastoid silent region 15824 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182809846..182809965) | | |
ID: 129993422 | ATAC-STARR-seq lymphoblastoid silent region 15823 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182806504..182806553) | | |
ID: 129993421 | ATAC-STARR-seq lymphoblastoid silent region 15822 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182806394..182806483) | | |
ID: 129993420 | ATAC-STARR-seq lymphoblastoid silent region 15821 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182448971..182449020) | | |
ID: 129993419 | ATAC-STARR-seq lymphoblastoid active region 22176 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182018888..182019397) | | |
ID: 129993418 | ATAC-STARR-seq lymphoblastoid active region 22175 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182018798..182018847) | | |
ID: 129993417 | ATAC-STARR-seq lymphoblastoid active region 22174 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (181971468..181971657) | | |
ID: 129993416 | ATAC-STARR-seq lymphoblastoid active region 22173 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (181830662..181830821) | | |
ID: 129661367 | ReSE screen-validated silencer GRCh37_chr4:183128595-183128794 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182207442..182207641) | | |
ID: 129661366 | ReSE screen-validated silencer GRCh37_chr4:182509195-182509349 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (181588042..181588196) | | |
ID: 127402003 | H3K4me1 hESC enhancer GRCh37_chr4:183818782-183819282 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182897629..182898129) | | |
ID: 127402002 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:183816185-183816755 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182895032..182895602) | | |
ID: 127402001 | H3K4me1 hESC enhancer GRCh37_chr4:183783677-183784250 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182862524..182863097) | | |
ID: 127402000 | NANOG-H3K4me1 hESC enhancer GRCh37_chr4:183783101-183783676 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182861948..182862523) | | |
ID: 127401999 | NANOG-H3K4me1 hESC enhancer GRCh37_chr4:183735292-183735847 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182814139..182814694) | | |
ID: 127401998 | H3K4me1 hESC enhancer GRCh37_chr4:183729853-183730354 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (182808700..182809201) | | |