| ID: 127898471 | H3K4me1 hESC enhancer GRCh37_chrX:152158397-152158896 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152989853..152990352) | | |
| ID: 127898470 | H3K4me1 hESC enhancer GRCh37_chrX:152084281-152084854 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152915737..152916310) | | |
| ID: 127898469 | H3K4me1 hESC enhancer GRCh37_chrX:152072629-152073160 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152904085..152904616) | | |
| ID: 127898468 | H3K4me1 hESC enhancer GRCh37_chrX:152070232-152070754 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152901688..152902210) | | |
| ID: 127898467 | H3K4me1 hESC enhancer GRCh37_chrX:152065863-152066363 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152897319..152897819) | | |
| ID: 126863347 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chrX:151987738-151988937 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152819194..152820393) | | |
| ID: 126863346 | CDK7 strongly-dependent group 2 enhancer GRCh37_chrX:151902449-151903648 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152733315..152734513) | | |
| ID: 126863345 | MED14-independent group 3 enhancer GRCh37_chrX:151599729-151600928 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152431257..152432456) | | |
| ID: 124905611 | uncharacterized LOC124905611 [Homo sapiens (human)] | | | |
| ID: 124905610 | uncharacterized LOC124905610 [Homo sapiens (human)] | | | |
| ID: 105373372 | uncharacterized LOC105373372 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152930255..152941573, complement) | | |
| ID: 102723547 | CSAG family member 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152708261..152709391, complement) | CSAG3B, CT24.2, TRAG-3, TRAG3 | 301096 |
| ID: 100420250 | MAGE family member A4 pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152682946..152683843) | | |
| ID: 100130935 | CSAG family member 4 (pseudogene) [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152733827..152740985) | | |
| ID: 768215 | microRNA 767 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152393421..152393529, complement) | MIRN767, hsa-mir-767, mir-767 | |
| ID: 406898 | microRNA 105-2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152394412..152394492, complement) | MIRN105-2, mir-105-2 | 300812 |
| ID: 406897 | microRNA 105-1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152392219..152392299, complement) | MIRN105-1, mir-105-1 | 300811 |
| ID: 402429 | keratin 8 pseudogene 8 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152479501..152481224) | | |
| ID: 389903 | CSAG family member 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152753921..152760219) | CSAG3A, CT24.2 | 301097 |
| ID: 266740 | MAGE family member A2B [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152714586..152718607) | CT1.2, MAGE2 | 300549 |