ID: 132090254 | Neanderthal introgressed variant-containing enhancer experimental_36177 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67163884..67164053) | | |
ID: 132090253 | Neanderthal introgressed variant-containing enhancer experimental_36142 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67091586..67091755) | | |
ID: 132090252 | Neanderthal introgressed variant-containing enhancer experimental_36114 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67049819..67049988) | | |
ID: 132090251 | Neanderthal introgressed variant-containing enhancer experimental_36038 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (66968110..66968279) | | |
ID: 132090250 | Neanderthal introgressed variant-containing enhancer experimental_35883 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (66821614..66821783) | | |
ID: 132090249 | Neanderthal introgressed variant-containing enhancer experimental_35856 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (66809656..66809825) | | |
ID: 130055892 | ATAC-STARR-seq lymphoblastoid active region 8578 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67359784..67360583) | | |
ID: 130055891 | ATAC-STARR-seq lymphoblastoid silent region 5855 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67241047..67242016) | | |
ID: 130055890 | ATAC-STARR-seq lymphoblastoid active region 8576 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67240787..67241066) | | |
ID: 130055889 | ATAC-STARR-seq lymphoblastoid active region 8575 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67108433..67108482) | | |
ID: 129663445 | ReSE screen-validated silencer GRCh37_chr14:67723162-67723330 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67256445..67256613) | | |
ID: 129390638 | MPRA-validated peak2181 silencer [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67277859..67278059) | | |
ID: 127827803 | H3K27ac hESC enhancer GRCh37_chr14:67825632-67826418 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67358915..67359763) | | |
ID: 127827802 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:67534507-67535036 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67067790..67068319) | | |
ID: 127827801 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:67533977-67534506 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67067260..67067789) | | |
ID: 127827800 | H3K27ac hESC enhancer GRCh37_chr14:67498602-67499102 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67031885..67032385) | | |
ID: 126861970 | MED14-independent group 3 enhancer GRCh37_chr14:67634697-67635896 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67167980..67169179) | | |
ID: 126861969 | MED14-independent group 3 enhancer GRCh37_chr14:67399728-67400927 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (66933011..66934210) | | |
ID: 124903330 | uncharacterized LOC124903330 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67228238..67241409, complement) | | |
ID: 121529650 | Sharpr-MPRA regulatory region 5377 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67187232..67187526) | | |