ID: 132090154 | Neanderthal introgressed variant-containing enhancer experimental_31500 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99359482..99359651) | | |
ID: 130008533 | ATAC-STARR-seq lymphoblastoid silent region 4761 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (100138751..100138900) | | |
ID: 130008532 | ATAC-STARR-seq lymphoblastoid silent region 4760 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99984909..99984958) | | |
ID: 130008531 | ATAC-STARR-seq lymphoblastoid silent region 4759 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99530142..99530211) | | |
ID: 130008530 | ATAC-STARR-seq lymphoblastoid silent region 4758 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99382185..99382284) | | |
ID: 130008529 | ATAC-STARR-seq lymphoblastoid active region 6850 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99131982..99132051) | | |
ID: 130008528 | ATAC-STARR-seq lymphoblastoid active region 6849 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99131232..99131281) | | |
ID: 129663210 | ReSE screen-validated silencer GRCh37_chr12:100414790-100414953 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (100021012..100021175) | | |
ID: 127824831 | H3K27ac hESC enhancer GRCh37_chr12:100536197-100536960 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (100142289..100143182) | | |
ID: 127824830 | H3K4me1 hESC enhancer GRCh37_chr12:100377744-100378574 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99983966..99984796) | | |
ID: 127824829 | NANOG-H3K4me1 hESC enhancer GRCh37_chr12:100117017-100117569 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99723239..99723791) | | |
ID: 127824828 | H3K27ac hESC enhancer GRCh37_chr12:100074143-100074643 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99680365..99680865) | | |
ID: 127824827 | OCT4-NANOG hESC enhancer GRCh37_chr12:100064333-100064865 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99670555..99671087) | | |
ID: 127824826 | NANOG-H3K27ac hESC enhancer GRCh37_chr12:99849451-99849950 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99455673..99456172) | | |
ID: 127824825 | NANOG-H3K27ac hESC enhancer GRCh37_chr12:99848949-99849450 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99455171..99455672) | | |
ID: 127824824 | H3K27ac hESC enhancer GRCh37_chr12:99548399-99548898 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99154621..99155120) | | |
ID: 127824823 | OCT4-NANOG hESC enhancer GRCh37_chr12:99502667-99503267 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99108889..99109489) | | |
ID: 101928937 | uncharacterized LOC101928937 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99093359..99105011) | | |
ID: 100873625 | RNA, 5S ribosomal pseudogene 366 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (99083783..99083905, complement) | RN5S366 | |
ID: 400064 | ribosomal protein S4X pseudogene 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (100008987..100009891, complement) | RPS4P1, RPS4X_6_1269 | |