ID: 132090571 | Neanderthal introgressed variant-containing enhancer experimental_59986 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17803178..17803347) | | |
ID: 132090570 | Neanderthal introgressed variant-containing enhancer experimental_59976 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17791224..17791393) | | |
ID: 130065459 | ATAC-STARR-seq lymphoblastoid active region 17566 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17682853..17682912) | | |
ID: 130065458 | ATAC-STARR-seq lymphoblastoid silent region 12698 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17682153..17682572) | | |
ID: 130065457 | ATAC-STARR-seq lymphoblastoid silent region 12697 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17681593..17681922) | | |
ID: 130065456 | ATAC-STARR-seq lymphoblastoid silent region 12694 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17651976..17652055) | | |
ID: 130065455 | ATAC-STARR-seq lymphoblastoid silent region 12693 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17649235..17649364) | | |
ID: 130065454 | ATAC-STARR-seq lymphoblastoid active region 17565 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17648226..17648315) | | |
ID: 130065453 | ATAC-STARR-seq lymphoblastoid silent region 12691 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17643895..17644024) | | |
ID: 129664569 | ReSE screen-validated silencer GRCh37_chr20:17782572-17782760 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17801927..17802115) | | |
ID: 127892665 | H3K4me1 hESC enhancer GRCh37_chr20:17876154-17876830 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17895510..17896186) | | |
ID: 127892664 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:17862693-17863606 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17882049..17882962) | | |
ID: 127892663 | H3K4me1 hESC enhancer GRCh37_chr20:17856497-17857399 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17875853..17876755) | | |
ID: 127892662 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:17851770-17852498 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17871126..17871854) | | |
ID: 127892661 | H3K4me1 hESC enhancer GRCh37_chr20:17839885-17840458 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17859241..17859814) | | |
ID: 127892660 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:17815795-17816372 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17835150..17835727) | | |
ID: 127892659 | H3K4me1 hESC enhancer GRCh37_chr20:17745451-17745952 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17764806..17765307) | | |
ID: 127892658 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr20:17733069-17733774 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17752424..17753129) | | |
ID: 127892657 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:17731191-17731743 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17750546..17751098) | | |
ID: 127892656 | H3K27ac hESC enhancer GRCh37_chr20:17661572-17662244 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (17680927..17681599) | | |