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: 124905611 | uncharacterized LOC124905611 [Homo sapiens (human)] | | | |
ID: 124905237 | uncharacterized LOC124905237 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152925349..152927158, complement) | | |
ID: 105373372 | uncharacterized LOC105373372 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152930255..152941573, complement) | | |
ID: 100420250 | MAGE family member A4 pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152682946..152683843) | | |
ID: 266740 | MAGE family member A2B [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152714586..152718607) | CT1.2, MAGE2 | 300549 |
ID: 139041 | MAGE family member A4 pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152784304..152789417, complement) | | |
ID: 114824 | PNMA family member 5 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152988824..152994116, complement) | | 300916 |
ID: 50814 | NAD(P) dependent steroid dehydrogenase-like [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152831063..152869729) | H105E3, SDR31E1, XAP104 | 300275 |
ID: 7739 | zinc finger protein 185 with LIM domain [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152898067..152973481) | SCELL | 300381 |
ID: 4101 | MAGE family member A2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152749863..152753884, complement) | CT1.2, MAGE2A, MAGEA2 | 300173 |
ID: 1069 | centrin 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152826994..152830757, complement) | CALT, CEN2 | 300006 |