ID: 130007178 | ATAC-STARR-seq lymphoblastoid silent region 4127 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (2034942..2035231) | | |
ID: 130007177 | ATAC-STARR-seq lymphoblastoid active region 5813 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (2004503..2004732) | | |
ID: 127823307 | OCT4-NANOG hESC enhancer GRCh37_chr12:2120775-2121283 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (2011609..2012117) | | |
ID: 127823306 | H3K27ac hESC enhancer GRCh37_chr12:2112705-2113344 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (2003539..2004178) | | |
ID: 127823305 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:2042322-2042920 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (1933156..1933754) | | |
ID: 127823304 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:2025891-2026467 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (1916725..1917301) | | |
ID: 127823303 | H3K4me1 hESC enhancer GRCh37_chr12:2021735-2022235 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (1912569..1913069) | | |
ID: 126861416 | MED14-independent group 3 enhancer GRCh37_chr12:2063223-2064422 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (1954057..1955256) | | |
ID: 124902858 | uncharacterized LOC124902858 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (1884206..1889442) | | |
ID: 124625880 | Sharpr-MPRA regulatory region 10568 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (1993463..1993757) | | |
ID: 107984540 | CACNA1C intronic transcript 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (2016671..2028839) | | |
ID: 100874369 | CACNA1C intronic transcript 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (2048352..2049463) | | |
ID: 100271702 | long intergenic non-protein coding RNA 940 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (1929202..1936576, complement) | | |
ID: 196513 | decapping mRNA 1B [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (1941591..2004457, complement) | DCP1 | 609843 |
ID: 93589 | calcium voltage-gated channel auxiliary subunit alpha2delta 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (1791963..1918652, complement) | RCD4 | 608171 |
ID: 775 | calcium voltage-gated channel subunit alpha1 C [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (1970780..2697950) | CACH2, CACN2-IT2, CACNL1A1, CCHL1A1, CaV1.2, LQT8, NEDHLSS, TS, TS. LQT8, CACNA1C | 114205 |