ID: 130065639 | ATAC-STARR-seq lymphoblastoid active region 17712 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32205749..32205798) | | |
ID: 130065638 | ATAC-STARR-seq lymphoblastoid silent region 12777 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32190168..32190447) | | |
ID: 130065637 | ATAC-STARR-seq lymphoblastoid active region 17711 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32133282..32133441) | | |
ID: 129664591 | ReSE screen-validated silencer GRCh37_chr20:30779125-30779322 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32191322..32191519) | | |
ID: 129664590 | ReSE screen-validated silencer GRCh37_chr20:30768259-30768439 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32180456..32180636) | | |
ID: 127892946 | H3K27ac hESC enhancer GRCh37_chr20:30795517-30796430 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32207530..32208627) | | |
ID: 127892945 | H3K4me1 hESC enhancer GRCh37_chr20:30784106-30784868 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32196303..32197065) | | |
ID: 127892944 | H3K4me1 hESC enhancer GRCh37_chr20:30776057-30776872 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32188254..32189069) | | |
ID: 127892943 | H3K27ac hESC enhancer GRCh37_chr20:30769860-30770360 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32182057..32182557) | | |
ID: 127892942 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:30763485-30764084 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32175682..32176281) | | |
ID: 127892941 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:30762883-30763484 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32175080..32175681) | | |
ID: 127892940 | H3K4me1 hESC enhancer GRCh37_chr20:30752983-30753483 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32165180..32165680) | | |
ID: 127892939 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:30747197-30748088 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32159394..32160285) | | |
ID: 127892938 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:30737033-30737924 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32149230..32150121) | | |
ID: 127892937 | NANOG-H3K27ac hESC enhancer GRCh37_chr20:30708941-30709834 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32121138..32122031) | | |
ID: 126863012 | MED14-independent group 3 enhancer GRCh37_chr20:30696834-30698033 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32109031..32110720) | | |
ID: 124904884 | uncharacterized LOC124904884 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32224369..32231041, complement) | | |
ID: 121853003 | Sharpr-MPRA regulatory region 8915 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32168546..32168840) | | |
ID: 112694702 | Sharpr-MPRA regulatory region 10464 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32152846..32153140) | | |
ID: 140757 | ribosomal L24 domain containing 1 pseudogene 6 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32170298..32170778, complement) | RPL24P1, dJ836N17.3 | |