ID: 128966711 | uncharacterized LOC128966711 [Homo sapiens (human)] | | | |
ID: 127889741 | H3K4me1 hESC enhancer GRCh37_chr18:77576519-77577020 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79816519..79817020) | | |
ID: 127889740 | H3K4me1 hESC enhancer GRCh37_chr18:77557221-77557817 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79797221..79797988) | | |
ID: 127889739 | H3K4me1 hESC enhancer GRCh37_chr18:77458305-77458804 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79698305..79698804) | | |
ID: 127889738 | H3K4me1 hESC enhancer GRCh37_chr18:77457803-77458304 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79697803..79698304) | | |
ID: 127889737 | H3K4me1 hESC enhancer GRCh37_chr18:77442069-77442575 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79682069..79682575) | | |
ID: 127889736 | H3K4me1 hESC enhancer GRCh37_chr18:77441560-77442068 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79681560..79682068) | | |
ID: 127889735 | H3K27ac hESC enhancer GRCh37_chr18:77439436-77439944 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79679436..79679944) | | |
ID: 127889734 | H3K27ac hESC enhancer GRCh37_chr18:77438928-77439435 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79678928..79679435) | | |
ID: 127889733 | H3K4me1 hESC enhancer GRCh37_chr18:77417519-77418054 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79657519..79658054) | | |
ID: 127889732 | H3K4me1 hESC enhancer GRCh37_chr18:77416983-77417518 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79656983..79657518) | | |
ID: 124908038 | uncharacterized LOC124908038 [Homo sapiens (human)] | | | |
ID: 284241 | CTDP1 divergent transcript [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79638928..79679745, complement) | | |
ID: 26251 | potassium voltage-gated channel modifier subfamily G member 2 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79797938..79900100) | KCNF2, KV6.2 | 605696 |
ID: 9150 | CTD phosphatase subunit 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79676768..79756625) | CCFDN, FCP1 | 604927 |