| ID: 130068069 | ATAC-STARR-seq lymphoblastoid active region 29506 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24647543..24647592) | | |
| ID: 130068068 | ATAC-STARR-seq lymphoblastoid silent region 20720 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24561259..24561418) | | |
| ID: 130068067 | ATAC-STARR-seq lymphoblastoid active region 29505 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24513341..24513460) | | |
| ID: 130068066 | ATAC-STARR-seq lymphoblastoid silent region 20719 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24465027..24465346) | | |
| ID: 127897319 | NANOG-H3K27ac hESC enhancer GRCh37_chrX:24546669-24547275 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24528552..24529158) | | |
| ID: 127897318 | H3K27ac hESC enhancer GRCh37_chrX:24546061-24546668 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24527944..24528551) | | |
| ID: 127897317 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:24509351-24510314 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24491234..24492197) | | |
| ID: 127897316 | NANOG hESC enhancer GRCh37_chrX:24428490-24429048 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24410373..24410931) | | |
| ID: 127897315 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:24394111-24394637 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24375994..24376520) | | |
| ID: 127897314 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chrX:24389623-24390398 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24371506..24372281) | | |
| ID: 127897313 | H3K4me1 hESC enhancer GRCh37_chrX:24382719-24383459 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24364602..24365342) | | |
| ID: 115482717 | H2B histone pseudogene 7 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24632257..24632601) | | |
| ID: 100874416 | SNRPE pseudogene 9 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24513407..24513682) | | |
| ID: 100874088 | PCYT1B antisense RNA 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24650073..24658237) | | |
| ID: 100130302 | SUPT20H like 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24360639..24367839) | FAM48B1, SPT20L | |
| ID: 729188 | ribosomal protein S26 pseudogene 58 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24429504..24429949, complement) | RPS26_33_1769 | |
| ID: 9468 | phosphate cytidylyltransferase 1B, choline [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24558087..24672887, complement) | CCTB, CTB | 300948 |
| ID: 5165 | pyruvate dehydrogenase kinase 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (24465286..24550466) | CMTX6, GS1-358P8.4 | 300906 |