| ID: 130068381 | ATAC-STARR-seq lymphoblastoid active region 29717 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65751071..65751130) | | |
| ID: 130068380 | ATAC-STARR-seq lymphoblastoid active region 29716 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65706586..65706645) | | |
| ID: 130068379 | ATAC-STARR-seq lymphoblastoid active region 29715 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65698399..65698628) | | |
| ID: 130068378 | ATAC-STARR-seq lymphoblastoid silent region 20882 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65688525..65688574) | | |
| ID: 130068377 | ATAC-STARR-seq lymphoblastoid silent region 20881 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65667346..65667675) | | |
| ID: 130068376 | ATAC-STARR-seq lymphoblastoid active region 29714 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65601917..65602036) | | |
| ID: 130068375 | ATAC-STARR-seq lymphoblastoid active region 29713 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65534882..65535061) | | |
| ID: 129664960 | ReSE screen-validated silencer GRCh37_chrX:64972237-64972435 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65752395..65752593) | | |
| ID: 129664959 | ReSE screen-validated silencer GRCh37_chrX:64924017-64924189 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65704155..65704327) | | |
| ID: 127897707 | H3K4me1 hESC enhancer GRCh37_chrX:64722693-64723193 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65502813..65503313) | | |
| ID: 127897706 | H3K4me1 hESC enhancer GRCh37_chrX:64722192-64722692 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65502312..65502812) | | |
| ID: 127897705 | OCT4-NANOG hESC enhancer GRCh37_chrX:64713210-64713789 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65493330..65493909) | | |
| ID: 125467759 | Sharpr-MPRA regulatory region 13592 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65722787..65723081) | | |
| ID: 645388 | AP1M2 pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65469085..65470579) | | |
| ID: 349386 | Nanog homeobox pseudogene 9 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65771763..65773832, complement) | NANOGP6 | |
| ID: 340554 | zinc finger CCCH-type containing 12B [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65034826..65507887) | CXorf32, MCPIP2 | 300889 |
| ID: 83957 | FERM domain containing 8 pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65550622..65552421, complement) | | |
| ID: 81887 | LAS1 like ribosome biogenesis factor [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65512582..65534787, complement) | Las1, Las1-like, MRXSWTS, WTS, dJ475B7.2 | 300964 |
| ID: 4478 | moesin [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65588377..65741931) | HEL70, IMD50 | 309845 |