ID: 127898273 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chrX:128851647-128852238 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129717670..129718261) | | |
ID: 127898272 | H3K4me1 hESC enhancer GRCh37_chrX:128783931-128784430 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129649954..129650453) | | |
ID: 127898271 | H3K4me1 hESC enhancer GRCh37_chrX:128783429-128783930 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129649452..129649953) | | |
ID: 124905214 | uncharacterized LOC124905214 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129718124..129728889) | | |
ID: 113875009 | Sharpr-MPRA regulatory region 14523 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129666332..129666626) | | |
ID: 105373334 | uncharacterized LOC105373334 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129675888..129678470, complement) | | |
ID: 8862 | apelin [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129645259..129654956, complement) | APEL, XNPEP2 | 300297 |