| ID: 132090049 | Neanderthal introgressed variant-containing enhancer experimental_25816 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130251829..130251998) | | |
| ID: 132090048 | Neanderthal introgressed variant-containing enhancer experimental_25789 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130243466..130243635) | | |
| ID: 132090047 | Neanderthal introgressed variant-containing enhancer experimental_25764 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130191000..130191169) | | |
| ID: 132090046 | Neanderthal introgressed variant-containing enhancer experimental_25722 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130145973..130146142) | | |
| ID: 132090045 | Neanderthal introgressed variant-containing enhancer experimental_25704 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130138128..130138297) | | |
| ID: 132090044 | Neanderthal introgressed variant-containing enhancer experimental_25699 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130137174..130137343) | | |
| ID: 127825696 | H3K4me1 hESC enhancer GRCh37_chr12:130682728-130683228 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130198183..130198683) | | |
| ID: 127825695 | H3K4me1 hESC enhancer GRCh37_chr12:130677479-130677979 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130192934..130193434) | | |
| ID: 127825694 | H3K4me1 hESC enhancer GRCh37_chr12:130667832-130668510 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130183287..130183965) | | |
| ID: 127825693 | NANOG hESC enhancer GRCh37_chr12:130649290-130649835 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130164745..130165290) | | |
| ID: 127825692 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:130648209-130649204 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130163664..130164659) | | |
| ID: 127825691 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:130646056-130646622 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130161511..130162077) | | |
| ID: 127825690 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:130645489-130646055 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130160944..130161510) | | |
| ID: 124903088 | uncharacterized LOC124903088 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130133382..130140832) | | |
| ID: 124849283 | Sharpr-MPRA regulatory region 11699 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130195964..130196258) | | |
| ID: 107984480 | uncharacterized LOC107984480 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130316210..130317397, complement) | | |
| ID: 100271562 | ribosomal protein S20 pseudogene 30 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130216807..130217157, complement) | RPS20_14_1295 | |
| ID: 440119 | FZD10 antisense divergent transcript [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130151593..130161678, complement) | FZD10-DT | |
| ID: 11211 | frizzled class receptor 10 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130162464..130165740) | CD350, FZ-10, Fz10, FzE7, hFz10 | 606147 |