| ID: 132090030 | Neanderthal introgressed variant-containing enhancer experimental_24865 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114158044..114158213) | | |
| ID: 132090029 | Neanderthal introgressed variant-containing enhancer experimental_24844 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114147882..114148051) | | |
| ID: 129663247 | ReSE screen-validated silencer GRCh37_chr12:114676508-114676718 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114238703..114238913) | | |
| ID: 127825179 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:114881262-114881765 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114443457..114443960) | | |
| ID: 127825178 | H3K4me1 hESC enhancer GRCh37_chr12:114878692-114879313 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114440887..114441508) | | |
| ID: 127825177 | H3K4me1 hESC enhancer GRCh37_chr12:114878069-114878691 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114440264..114440886) | | |
| ID: 127825176 | H3K4me1 hESC enhancer GRCh37_chr12:114876822-114877445 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114439017..114439640) | | |
| ID: 127825175 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:114847097-114847637 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114409292..114409832) | | |
| ID: 127825174 | H3K4me1 hESC enhancer GRCh37_chr12:114843876-114844376 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114406071..114406571) | | |
| ID: 127825173 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:114843151-114843837 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114405346..114406032) | | |
| ID: 127825172 | NANOG-H3K4me1 hESC enhancer GRCh37_chr12:114773645-114774145 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114335840..114336340) | | |
| ID: 127825171 | H3K4me1 hESC enhancer GRCh37_chr12:114740105-114740631 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114302300..114302826) | | |
| ID: 127825170 | H3K4me1 hESC enhancer GRCh37_chr12:114739578-114740104 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114301773..114302299) | | |
| ID: 127825169 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:114723717-114724462 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114285912..114286657) | | |
| ID: 126861644 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr12:114601036-114602235 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114163231..114164430) | | |
| ID: 112136112 | Sharpr-MPRA regulatory region 11920 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114242004..114242298) | | |
| ID: 109280165 | CRE16 enhancer upstream of TBX5 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114415466..114420433) | | |
| ID: 109280163 | CRE9 enhancer downstream of TBX5 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114263402..114266886) | | |
| ID: 106479190 | RN7SK pseudogene 216 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114504876..114505187, complement) | | |
| ID: 105369998 | uncharacterized LOC105369998 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114414357..114448581, complement) | | |