ID: 130007807 | ATAC-STARR-seq lymphoblastoid silent region 4416 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48969959..48970038) | | |
ID: 130007806 | ATAC-STARR-seq lymphoblastoid active region 6297 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48956735..48956814) | | |
ID: 130007805 | ATAC-STARR-seq lymphoblastoid silent region 4415 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48936489..48936678) | | |
ID: 130007804 | ATAC-STARR-seq lymphoblastoid active region 6296 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48925758..48925857) | | |
ID: 130007803 | ATAC-STARR-seq lymphoblastoid active region 6295 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48924438..48924497) | | |
ID: 130007802 | ATAC-STARR-seq lymphoblastoid silent region 4414 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48904090..48904139) | | |
ID: 129663134 | ReSE screen-validated silencer GRCh37_chr12:49353706-49353915 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48959923..48960132) | | |
ID: 129663133 | ReSE screen-validated silencer GRCh37_chr12:49340991-49341204 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48947208..48947421) | | |
ID: 127824091 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:49361393-49362276 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48967610..48968493) | | |
ID: 127824090 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:49360112-49360664 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48966329..48966881) | | |
ID: 127824089 | H3K27ac hESC enhancer GRCh37_chr12:49358123-49358716 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48964340..48964933) | | |
ID: 127824088 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:49349467-49350462 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48955684..48956679) | | |
ID: 127824087 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:49341223-49341815 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48947440..48948032) | | |
ID: 127824086 | H3K4me1 hESC enhancer GRCh37_chr12:49338542-49339042 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48944759..48945259) | | |
ID: 124903110 | small nucleolar RNA U13 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48960738..48960836, complement) | | |
ID: 124629349 | Sharpr-MPRA regulatory region 4091 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48971506..48971800) | | |
ID: 100271306 | ribosomal protein L32 pseudogene 27 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48903368..48903818, complement) | RPL32_7_1234 | |
ID: 85478 | coiled-coil domain containing 65 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48904133..48921576) | CFAP250, DRC2, FAP250, NYD-SP28 | 611088 |
ID: 51303 | FKBP prolyl isomerase 11 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48921963..48939034, complement) | FKBP19 | 610571 |
ID: 7480 | Wnt family member 10B [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48965340..48971735, complement) | SHFM6, STHAG8, WNT-12 | 601906 |