| ID: 129663404 | ReSE screen-validated silencer GRCh37_chr14:21817331-21817510 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21349172..21349351) | | |
| ID: 127827205 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr14:21777043-21777570 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21308884..21309411) | | |
| ID: 127827204 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:21737705-21738330 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21269533..21270171) | | |
| ID: 127827203 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:21737080-21737704 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21268921..21269545) | | |
| ID: 127827202 | H3K27ac hESC enhancer GRCh37_chr14:21735001-21735580 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21266842..21267421) | | |
| ID: 127827201 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:21734420-21735000 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21266261..21266841) | | |
| ID: 127827200 | H3K4me1 hESC enhancer GRCh37_chr14:21722469-21723406 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21254310..21255247) | | |
| ID: 127827199 | H3K27ac hESC enhancer GRCh37_chr14:21686859-21687402 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21218700..21219243) | | |
| ID: 126861888 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr14:21859227-21860426 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21391068..21392267) | | |
| ID: 126861887 | BRD4-independent group 4 enhancer GRCh37_chr14:21820143-21821342 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21351984..21353183) | | |
| ID: 107984643 | uncharacterized LOC107984643 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21384273..21391806) | | |
| ID: 692053 | small nucleolar RNA, C/D box 9 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21392151..21392253, complement) | mgU6-53B | |
| ID: 359759 | mitochondrial ribosomal protein S17 pseudogene 6 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21291239..21291583) | | |
| ID: 283624 | long intergenic non-protein coding RNA 641 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21200079..21206900, complement) | | |
| ID: 57680 | chromodomain helicase DNA binding protein 8 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21385199..21456123, complement) | AUTS18, HELSNF1, IDDAM | 610528 |
| ID: 57096 | RPGR interacting protein 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21280083..21351301) | CORD13, LCA6, RGI1, RGRIP, RPGRIPd, RPGRIP1 | 605446 |
| ID: 11198 | SPT16 homolog, facilitates chromatin remodeling subunit [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21351476..21384019, complement) | CDC68, FACTP140, NEDDFAC, SPT16, SPT16/CDC68 | 605012 |
| ID: 3183 | heterogeneous nuclear ribonucleoprotein C [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21209147..21269442, complement) | C1, C2, HNRNP, HNRPC, MRD74, SNRPC | 164020 |