ID: 127897393 | H3K4me1 hESC enhancer GRCh37_chrX:34175554-34176054 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (34157437..34157937) | | |
ID: 127897392 | H3K4me1 hESC enhancer GRCh37_chrX:34165078-34165618 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (34146961..34147501) | | |
ID: 127897391 | H3K4me1 hESC enhancer GRCh37_chrX:33987093-33987592 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (33968976..33969475) | | |
ID: 127897390 | OCT4-NANOG hESC enhancer GRCh37_chrX:33926163-33926715 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (33908046..33908598) | | |
ID: 105373153 | uncharacterized LOC105373153 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (33726366..34077114) | | |
ID: 158724 | family with sequence similarity 47 member A [Homo sapiens (human)] | Chromosome X, NC_000023.11 (34129752..34132314, complement) | | |
ID: 139431 | ferritin heavy chain 1 pseudogene 14 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (34147040..34147753) | | |