ID: 127889177 | NANOG hESC enhancer GRCh37_chr18:42915554-42916119 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (45335589..45336154) | | |
ID: 127889176 | H3K4me1 hESC enhancer GRCh37_chr18:42589119-42589618 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (45009154..45009653) | | |
ID: 126862735 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr18:42982182-42983381 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (45402217..45403416) | | |
ID: 110121371 | VISTA enhancer hs1464 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (45553091..45555264) | | |
ID: 110121367 | VISTA enhancer hs1440 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (45588382..45590764) | | |
ID: 110121353 | VISTA enhancer hs1363 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (45362398..45364170) | | |
ID: 105372093 | uncharacterized LOC105372093 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (45606336..45782836, complement) | | |
ID: 105372092 | uncharacterized LOC105372092 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (45713149..45723035) | | |
ID: 105372091 | uncharacterized LOC105372091 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (45069276..45156484, complement) | | |
ID: 101927980 | SLC14A2 antisense RNA 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (45364887..45507063, complement) | | |
ID: 101927961 | uncharacterized LOC101927961 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (45158556..45181368, complement) | | |
ID: 26040 | SET binding protein 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (44680073..45068510) | MRD29, SEB | 611060 |
ID: 8170 | solute carrier family 14 member 2 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (45167963..45683688) | HUT2, UT-A2, UT2, UTA, UTR, hUT-A6 | 601611 |
ID: 6563 | solute carrier family 14 member 1 (Kidd blood group) [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (45724181..45752520) | HUT11, HUT11A, HsT1341, JK, Jk(a), Jk(b), RACH1, RACH2, UT-B1, UT1, UTE | 613868 |