ID: 130055849 | ATAC-STARR-seq lymphoblastoid silent region 5846 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (65020021..65020070) | | |
ID: 130055848 | ATAC-STARR-seq lymphoblastoid active region 8540 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64990528..64990647) | | |
ID: 130055847 | ATAC-STARR-seq lymphoblastoid silent region 5845 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64972129..64972498) | | |
ID: 130055846 | ATAC-STARR-seq lymphoblastoid active region 8539 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64929005..64929074) | | |
ID: 130055845 | ATAC-STARR-seq lymphoblastoid active region 8538 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64914455..64914724) | | |
ID: 129390632 | MPRA-validated peak2167 silencer [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64926478..64926678) | | |
ID: 127827773 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:65544121-65545096 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (65077403..65078378) | | |
ID: 127827772 | H3K4me1 hESC enhancer GRCh37_chr14:65448241-65448742 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64981523..64982024) | | |
ID: 127827771 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:65441391-65442168 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64974673..64975450) | | |
ID: 127827770 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:65426829-65427347 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64960111..64960629) | | |
ID: 127827769 | H3K4me1 hESC enhancer GRCh37_chr14:65421611-65422488 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64954893..64955770) | | |
ID: 126861966 | MED14-independent group 3 enhancer GRCh37_chr14:65471811-65473010 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (65005093..65006292) | | |
ID: 107984655 | uncharacterized LOC107984655 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64985539..64987113, complement) | | |
ID: 100616490 | microRNA 4706 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (65044688..65044769) | mir-4706 | |
ID: 100529261 | CHURC1-FNTB readthrough [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64914361..65062655) | FNTB, FTase-beta | |
ID: 100506321 | uncharacterized LOC100506321 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (65089918..65094311) | | |
ID: 376267 | RAB15, member RAS oncogene family [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64945816..64972336, complement) | | 619547 |
ID: 91612 | churchill domain containing 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64914455..64935368) | C14orf52, My015, chch | 608577 |
ID: 4149 | MYC associated factor X [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (65006101..65102695, complement) | PDMCS, bHLHd4 | 154950 |
ID: 2877 | glutathione peroxidase 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64939158..64942745, complement) | GI-GPx, GPRP, GPRP-2, GPx-2, GPx-GI, GSHPX-GI, GSHPx-2 | 138319 |