ID: 130008482 | ATAC-STARR-seq lymphoblastoid silent region 4739 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95623709..95623778) | | |
ID: 130008481 | ATAC-STARR-seq lymphoblastoid active region 6811 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95574125..95574254) | | |
ID: 130008480 | ATAC-STARR-seq lymphoblastoid active region 6810 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95473969..95474368) | | |
ID: 129663204 | ReSE screen-validated silencer GRCh37_chr12:95846624-95846848 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95452848..95453072) | | |
ID: 129390535 | MPRA-validated peak1899 silencer [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95519060..95519260) | | |
ID: 127824775 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:96016523-96017477 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95622747..95623701) | | |
ID: 127824774 | H3K27ac hESC enhancer GRCh37_chr12:96008766-96009393 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95614990..95615617) | | |
ID: 127824773 | NANOG-H3K27ac hESC enhancer GRCh37_chr12:96005509-96006077 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95611733..95612301) | | |
ID: 127824772 | H3K27ac hESC enhancer GRCh37_chr12:96004940-96005508 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95611164..95611732) | | |
ID: 127824771 | H3K27ac hESC enhancer GRCh37_chr12:95936387-95936886 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95542611..95543110) | | |
ID: 127824770 | H3K27ac hESC enhancer GRCh37_chr12:95916458-95916958 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95522682..95523182) | | |
ID: 126861602 | MED14-independent group 3 enhancer GRCh37_chr12:96026735-96027934 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95632959..95634158) | | |
ID: 124646384 | Sharpr-MPRA regulatory region 15569 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95653893..95654187) | | |
ID: 107984545 | uncharacterized LOC107984545 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95407939..95448699, complement) | | |
ID: 106481412 | RNA, U6 small nuclear 735, pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95438737..95438843, complement) | | |
ID: 100132594 | phosphoglycerate mutase 1 pseudogene 5 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95649255..95673999) | | |
ID: 643531 | ribosomal protein L29 pseudogene 26 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95467273..95467876, complement) | RPL29_14_1268 | |
ID: 84101 | ubiquitin specific peptidase 44 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95516560..95551681, complement) | | 610993 |
ID: 59277 | netrin 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95657807..95791155, complement) | PRO3091 | 610401 |
ID: 10988 | methionyl aminopeptidase 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95474152..95515839) | MAP2, MNPEP, p67eIF2 | 601870 |