ID: 132089942 | Neanderthal introgressed variant-containing enhancer experimental_21658 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (69852203..69852372) | | |
ID: 130006295 | ATAC-STARR-seq lymphoblastoid silent region 3699 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70203706..70203785) | | |
ID: 130006294 | ATAC-STARR-seq lymphoblastoid active region 5161 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70191913..70191972) | | |
ID: 129662986 | ReSE screen-validated silencer GRCh37_chr11:70049941-70050132 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70203835..70204026) | | |
ID: 129662985 | ReSE screen-validated silencer GRCh37_chr11:70008633-70008799 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70162527..70162693) | | |
ID: 129662984 | ReSE screen-validated silencer GRCh37_chr11:69938122-69938334 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70092016..70092228) | | |
ID: 129662983 | ReSE screen-validated silencer GRCh37_chr11:69935765-69935935 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70089659..70089829) | | |
ID: 129662982 | ReSE screen-validated silencer GRCh37_chr11:69918266-69918443 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70072160..70072337) | | |
ID: 129662981 | ReSE screen-validated silencer GRCh37_chr11:69871617-69872015 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70025511..70025909) | | |
ID: 129390301 | MPRA-validated peak1329 silencer [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (69838027..69838227) | | |
ID: 127821855 | H3K27ac hESC enhancer GRCh37_chr11:70042837-70043336 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70196731..70197230) | | |
ID: 127821854 | H3K4me1 hESC enhancer GRCh37_chr11:70020559-70021264 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70174453..70175158) | | |
ID: 127821853 | H3K4me1 hESC enhancer GRCh37_chr11:70017141-70017640 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70171035..70171534) | | |
ID: 127821852 | H3K4me1 hESC enhancer GRCh37_chr11:70016639-70017140 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70170533..70171034) | | |
ID: 127821851 | H3K4me1 hESC enhancer GRCh37_chr11:70001951-70002451 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70155845..70156345) | | |
ID: 127821850 | H3K4me1 hESC enhancer GRCh37_chr11:70001450-70001950 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70155344..70155844) | | |
ID: 127821849 | NANOG-H3K4me1 hESC enhancer GRCh37_chr11:69987699-69988510 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70141593..70142404) | | |
ID: 127821848 | NANOG-H3K4me1 hESC enhancer GRCh37_chr11:69986885-69987698 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70140779..70141592) | | |
ID: 127821847 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:69974897-69975729 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70128791..70129623) | | |
ID: 127821846 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:69969469-69970107 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (70123363..70124001) | | |