ID: 127897191 | OCT4-NANOG hESC enhancer GRCh37_chrX:10579147-10580022 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10611107..10611982) | | |
ID: 127897190 | OCT4-NANOG hESC enhancer GRCh37_chrX:10476778-10477647 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10508738..10509607) | | |
ID: 127897189 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:10141885-10142861 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10173845..10174821) | | |
ID: 126863208 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chrX:10602208-10603407 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10634168..10635367) | | |
ID: 126863207 | BRD4-independent group 4 enhancer GRCh37_chrX:10416979-10418178 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10448939..10450138) | | |
ID: 125446270 | Sharpr-MPRA regulatory region 5514 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10722829..10723123) | | |
ID: 124905245 | uncharacterized LOC124905245 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10619701..10622924) | | |
ID: 124905244 | uncharacterized LOC124905244 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10900966..10929484) | | |
ID: 124905243 | uncharacterized LOC124905243 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10949805..10964704) | | |
ID: 121853050 | Sharpr-MPRA regulatory region 6238 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10922189..10922483) | | |
ID: 121627958 | Sharpr-MPRA regulatory region 7563 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10119429..10119723) | | |
ID: 111242786 | MID1 promoter D [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10589855..10590337) | | |
ID: 106481433 | RNA, U6 small nuclear 800, pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10582817..10582919) | | |
ID: 55841 | WWC family member 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10015254..10144474) | BM042 | 301089 |
ID: 4281 | midline 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10445310..10833683, complement) | BBBG1, FXY, GBBB, GBBB1, MIDIN, OGS1, OS, OSX, RNF59, TRIM18, XPRF, ZNFXY | 300552 |
ID: 1183 | chloride voltage-gated channel 4 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10156975..10237660) | CLC4, ClC-4, ClC-4A, MRX15, MRX49, MRXSRC | 302910 |