| ID: 129664923 | ReSE screen-validated silencer GRCh37_chrX:30300409-30300510 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30282292..30282393) | | |
| ID: 129664922 | ReSE screen-validated silencer GRCh37_chrX:30274564-30274739 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30256447..30256622) | | |
| ID: 127897370 | H3K4me1 hESC enhancer GRCh37_chrX:30326716-30327216 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30308599..30309099) | | |
| ID: 127897369 | NANOG hESC enhancer GRCh37_chrX:30259792-30260365 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30241675..30242248) | | |
| ID: 127897368 | NANOG hESC enhancer GRCh37_chrX:30246492-30247101 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30228375..30228984) | | |
| ID: 127897367 | OCT4-NANOG hESC enhancer GRCh37_chrX:30237442-30238027 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30219325..30219910) | | |
| ID: 127897366 | H3K4me1 hESC enhancer GRCh37_chrX:30236871-30237370 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30218754..30219253) | | |
| ID: 126863236 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chrX:30232864-30234063 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30214747..30215946) | | |
| ID: 116309150 | CRISPRi-validated cis-regulatory element chrX.505 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30284257..30284403) | | |
| ID: 116309149 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chrX:30301194-30302393 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30283077..30284276) | | |
| ID: 108410393 | NR0B1 5' regulatory region [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30309364..30314190) | | |
| ID: 100420075 | phospholipase C epsilon 1 pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30289853..30290358, complement) | | |
| ID: 4115 | MAGE family member B4 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30242000..30244187) | CT3.6 | 300153 |
| ID: 4114 | MAGE family member B3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30230657..30237495) | CT3.5 | 300152 |
| ID: 4113 | MAGE family member B2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30215563..30220089) | CT3.2, DAM6, MAGE-XP-2 | 300098 |
| ID: 4112 | MAGE family member B1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30243731..30252040) | CT3.1, DAM10, MAGE-Xp, MAGEL1 | 300097 |
| ID: 190 | nuclear receptor subfamily 0 group B member 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30304206..30309390, complement) | AHC, AHCH, AHX, DAX-1, DAX1, DSS, GTD, HHG, NROB1, SRXY2 | 300473 |