ID: 127825052 | H3K4me1 hESC enhancer GRCh37_chr12:111124990-111125818 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (110687185..110688013) | | |
ID: 127825051 | H3K4me1 hESC enhancer GRCh37_chr12:111099215-111099717 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (110661410..110661912) | | |
ID: 127825050 | H3K4me1 hESC enhancer GRCh37_chr12:110978759-110979259 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (110540954..110541454) | | |
ID: 124903017 | uncharacterized LOC124903017 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (110662671..110672923) | | |
ID: 111465008 | HNF4 motif-containing MPRA enhancer 250 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (110575493..110575637) | | |
ID: 106481029 | RNA, 7SL, cytoplasmic 387, pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (110625645..110625917, complement) | | |
ID: 160760 | protein phosphatase targeting COQ7 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (110533245..110583318, complement) | TA-PP2C, TAPP2C | 609668 |
ID: 84329 | hydrogen voltage gated channel 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (110648686..110704952, complement) | HV1, VSOP | 611227 |
ID: 79600 | tectonic family member 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (110614129..110649430) | JBTS13, TECT1 | 609863 |