| ID: 130067991 | ATAC-STARR-seq lymphoblastoid active region 29454 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16719422..16719481) | | |
| ID: 130067990 | ATAC-STARR-seq lymphoblastoid silent region 20679 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16712452..16712541) | | |
| ID: 130067989 | ATAC-STARR-seq lymphoblastoid silent region 20678 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16712122..16712391) | | |
| ID: 127897242 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:16648498-16649144 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16630375..16631021) | | |
| ID: 127897241 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:16647850-16648497 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16629727..16630374) | | |
| ID: 127897240 | H3K4me1 hESC enhancer GRCh37_chrX:16625033-16625533 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16606910..16607410) | | |
| ID: 127897239 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:16604766-16605549 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16586643..16587426) | | |
| ID: 127897238 | NANOG-H3K27ac hESC enhancer GRCh37_chrX:16598415-16599261 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16580292..16581138) | | |
| ID: 127897237 | NANOG-H3K27ac hESC enhancer GRCh37_chrX:16597568-16598414 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16579445..16580291) | | |
| ID: 127897236 | OCT4-NANOG hESC enhancer GRCh37_chrX:16596905-16597407 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16578782..16579284) | | |
| ID: 127897235 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:16596400-16596904 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16578277..16578781) | | |
| ID: 127897234 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:16595896-16596399 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16577773..16578276) | | |
| ID: 127897233 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:16593879-16594382 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16575756..16576259) | | |
| ID: 125446273 | Sharpr-MPRA regulatory region 4999 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16733086..16733380) | | |
| ID: 106480524 | RNA, 7SL, cytoplasmic 658, pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16539137..16539439, complement) | | |
| ID: 100616428 | microRNA 548am [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16627012..16627085, complement) | | |
| ID: 100151651 | RNA, U7 small nuclear 56 pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16767845..16767903) | U7.56 | |
| ID: 94056 | synapse associated protein 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16719612..16765340) | BSTA, PRO3113 | |
| ID: 56474 | CTP synthase 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16587999..16712910, complement) | GATD5B | 300380 |
| ID: 795 | S100 calcium binding protein G [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16650158..16654670) | CABP, CABP1, CABP9K, CALB3 | 302020 |