ID: 132090293 | Neanderthal introgressed variant-containing enhancer experimental_38841 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96092173..96092342) | | |
ID: 130056396 | ATAC-STARR-seq lymphoblastoid active region 8983 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96126370..96126539) | | |
ID: 130056395 | ATAC-STARR-seq lymphoblastoid active region 8982 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96078108..96078157) | | |
ID: 130056394 | ATAC-STARR-seq lymphoblastoid active region 8981 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96052146..96052205) | | |
ID: 130056393 | ATAC-STARR-seq lymphoblastoid silent region 6052 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96039422..96039471) | | |
ID: 130056392 | ATAC-STARR-seq lymphoblastoid silent region 6051 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96039212..96039401) | | |
ID: 129663492 | ReSE screen-validated silencer GRCh37_chr14:96697669-96697864 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96231332..96231527) | | |
ID: 129663491 | ReSE screen-validated silencer GRCh37_chr14:96529045-96529222 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96062708..96062885) | | |
ID: 129663490 | ReSE screen-validated silencer GRCh37_chr14:96526720-96526873 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96060383..96060536) | | |
ID: 129390666 | MPRA-validated peak2244 silencer [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (95935319..95935519) | | |
ID: 127828459 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:96719533-96720042 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96253196..96253705) | | |
ID: 127828458 | H3K4me1 hESC enhancer GRCh37_chr14:96670637-96671512 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96204300..96205175) | | |
ID: 127828457 | H3K4me1 hESC enhancer GRCh37_chr14:96664109-96664715 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96197772..96198378) | | |
ID: 127828456 | H3K4me1 hESC enhancer GRCh37_chr14:96661711-96662318 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96195374..96195981) | | |
ID: 127828455 | H3K4me1 hESC enhancer GRCh37_chr14:96661103-96661710 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96194766..96195373) | | |
ID: 127828454 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:96660495-96661102 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96194158..96194765) | | |
ID: 127828453 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:96659886-96660494 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96193549..96194157) | | |
ID: 127828452 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:96658061-96658668 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96191724..96192331) | | |
ID: 127828451 | H3K4me1 hESC enhancer GRCh37_chr14:96642023-96642523 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96175686..96176186) | | |
ID: 127828450 | H3K4me1 hESC enhancer GRCh37_chr14:96563297-96563798 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96096960..96097461) | | |