ID: 130009119 | ATAC-STARR-seq lymphoblastoid active region 7275 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123767704..123767863) | | |
ID: 130009118 | ATAC-STARR-seq lymphoblastoid silent region 5050 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123761882..123762301) | | |
ID: 130009117 | ATAC-STARR-seq lymphoblastoid silent region 5049 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123712178..123712727) | | |
ID: 130009116 | ATAC-STARR-seq lymphoblastoid active region 7274 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123681639..123681688) | | |
ID: 130009115 | ATAC-STARR-seq lymphoblastoid active region 7273 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123633713..123633902) | | |
ID: 129663287 | ReSE screen-validated silencer GRCh37_chr12:124206184-124206364 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123721637..123721817) | | |
ID: 129663286 | ReSE screen-validated silencer GRCh37_chr12:124184156-124184331 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123699609..123699784) | | |
ID: 129663285 | ReSE screen-validated silencer GRCh37_chr12:124129599-124129794 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123645052..123645247) | | |
ID: 127825502 | H3K4me1 hESC enhancer GRCh37_chr12:124401655-124402156 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123917108..123917609) | | |
ID: 127825501 | H3K4me1 hESC enhancer GRCh37_chr12:124383373-124383873 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123898826..123899326) | | |
ID: 126861667 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr12:124402328-124403527 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123917781..123918980) | | |
ID: 126861666 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr12:124232793-124233992 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123748246..123749445) | | |
ID: 126861665 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr12:124143885-124145084 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123659338..123660537) | | |
ID: 124903043 | uncharacterized LOC124903043 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123922598..123925017, complement) | | |
ID: 112163535 | Sharpr-MPRA regulatory region 5794 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123907842..123908136) | | |
ID: 105370044 | uncharacterized LOC105370044 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123765168..123790927, complement) | | |
ID: 105370042 | uncharacterized LOC105370042 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123712766..123723090, complement) | | |
ID: 100271302 | ribosomal protein L27 pseudogene 12 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123721218..123721642, complement) | RPL27_4_1293 | |
ID: 196385 | dynein axonemal heavy chain 10 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123762301..123935720) | SPGF56 | 605884 |
ID: 79867 | tectonic family member 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123671113..123708399) | C12orf38, JBTS24, MKS8, TECT2 | 613846 |