ID: 127826665 | H3K4me1 hESC enhancer GRCh37_chr13:95365523-95366024 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94713269..94713770) | | |
ID: 127826664 | H3K4me1 hESC enhancer GRCh37_chr13:95357739-95358243 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94705485..94705989) | | |
ID: 127826663 | H3K4me1 hESC enhancer GRCh37_chr13:95357234-95357738 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94704980..94705484) | | |
ID: 127826662 | H3K4me1 hESC enhancer GRCh37_chr13:95354373-95355048 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94702119..94702794) | | |
ID: 127826661 | H3K4me1 hESC enhancer GRCh37_chr13:95353695-95354372 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94701441..94702118) | | |
ID: 127826660 | NANOG hESC enhancer GRCh37_chr13:95313022-95313523 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94660768..94661269) | | |
ID: 112268114 | uncharacterized LOC112268114 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94712720..94713443, complement) | | |
ID: 110120933 | VISTA enhancer hs796 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94661598..94663187) | | |
ID: 110120881 | VISTA enhancer hs488 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94706009..94707763) | | |
ID: 106479436 | RNA, 7SL, cytoplasmic 585, pseudogene [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94699223..94699502, complement) | | |
ID: 101927248 | long intergenic non-protein coding RNA 391 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94698725..94708501, complement) | | |
ID: 100873368 | RNA, 5S ribosomal pseudogene 36 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94651397..94651529, complement) | RN5S36 | |
ID: 100507533 | SOX21 antisense divergent transcript 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94712716..94715945) | | |
ID: 100129259 | bromodomain containing 7 pseudogene 5 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94757310..94759417, complement) | | |
ID: 11166 | SRY-box transcription factor 21 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94709622..94712545, complement) | SOX25 | 604974 |