| ID: 130068159 | ATAC-STARR-seq lymphoblastoid active region 29553 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41117043..41117102) | | |
| ID: 130068158 | ATAC-STARR-seq lymphoblastoid silent region 20772 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41086180..41086639) | | |
| ID: 130068157 | ATAC-STARR-seq lymphoblastoid silent region 20771 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41085100..41085479) | | |
| ID: 129664937 | ReSE screen-validated silencer GRCh37_chrX:41165064-41165269 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41305811..41306016) | | |
| ID: 129664936 | ReSE screen-validated silencer GRCh37_chrX:40973903-40974035 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41114650..41114782) | | |
| ID: 127897481 | NANOG hESC enhancer GRCh37_chrX:41163312-41163875 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41304059..41304622) | | |
| ID: 127897480 | NANOG-H3K27ac hESC enhancer GRCh37_chrX:41150473-41151037 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41291220..41291784) | | |
| ID: 127897479 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:41135579-41136079 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41276326..41276826) | | |
| ID: 127897478 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:41135078-41135578 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41275825..41276351) | | |
| ID: 127897477 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:41070375-41071092 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41211122..41211839) | | |
| ID: 127897476 | H3K27ac hESC enhancer GRCh37_chrX:40991170-40991670 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41131917..41132417) | | |
| ID: 127897475 | H3K27ac hESC enhancer GRCh37_chrX:40944771-40945308 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41085518..41086055) | | |
| ID: 113875024 | Sharpr-MPRA regulatory region 13807 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41084396..41084979) | | |
| ID: 105373185 | long intergenic non-protein coding RNA 2601 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41275739..41276778) | | |
| ID: 100873553 | RNA, 5S ribosomal pseudogene 502 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41292798..41292916) | RN5S502 | |
| ID: 643043 | SHISA5 pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41321413..41323574, complement) | | |
| ID: 442447 | chloride intracellular channel 4 pseudogene 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41076893..41077930) | | |
| ID: 8239 | ubiquitin specific peptidase 9 X-linked [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41085445..41236579) | DFFRX, FAF, FAF-X, FAM, MRX99, MRXS99F, XLID99, hFAM | 300072 |