| ID: 127885016 | H3K4me1 hESC enhancer GRCh37_chr16:87504708-87505665 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87471102..87472059) | | |
| ID: 127885015 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:87503438-87504022 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87469832..87470416) | | |
| ID: 127885014 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:87502852-87503437 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87469246..87469831) | | |
| ID: 127885013 | H3K4me1 hESC enhancer GRCh37_chr16:87486642-87487142 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87453036..87453536) | | |
| ID: 127885012 | H3K4me1 hESC enhancer GRCh37_chr16:87468667-87469584 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87435061..87435978) | | |
| ID: 127885011 | H3K4me1 hESC enhancer GRCh37_chr16:87460343-87460850 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87426737..87427244) | | |
| ID: 127885010 | H3K4me1 hESC enhancer GRCh37_chr16:87458817-87459326 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87425211..87425720) | | |
| ID: 127885009 | H3K4me1 hESC enhancer GRCh37_chr16:87457291-87457798 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87423685..87424192) | | |
| ID: 127885008 | H3K4me1 hESC enhancer GRCh37_chr16:87456781-87457290 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87423175..87423684) | | |
| ID: 126862438 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr16:87490779-87491978 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87457173..87458372) | | |
| ID: 23174 | zinc finger CCHC-type containing 14 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87406248..87493024, complement) | BDG-29, BDG29 | 620697 |
| ID: 2910 | nuclear receptor subfamily 3 group C member 1 pseudogene 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87467136..87467670) | GCR2, GCRL, GRLL1, NR3C1P | 138060 |