Tag | Content |
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EnhancerAtlas ID | HS187-11501 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr18:51796030-51797350 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr18:51797316-51797328 | GTTTGTTTGTTT | + | 6.32 | HES2 | MA0616.2 | chr18:51796677-51796687 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr18:51796677-51796687 | GGCACGTGCC | - | 6.02 | MEF2A | MA0052.3 | chr18:51797250-51797262 | GCTAAAAATAGC | + | 6.44 | MEF2B | MA0660.1 | chr18:51797250-51797262 | GCTAAAAATAGC | + | 6.92 | MEF2C | MA0497.1 | chr18:51797248-51797263 | GAGCTAAAAATAGCC | + | 6.83 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_58972 | chr18:51772671-51812936 | Ly3 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | GGTGCGCCGC AGCCAGAGGA GCCAGCGGCC TCCTTGGGTG TAAATGAGAA GGGTGGGGCA 60 GGCGGACGCT CGGGGCGGCG GCCACTGGGG CGCGACCGTC CCCGCCCCAC TCGGCTCCTC 120 TAAGAGAGGG CTGCCTCCCT CTGCCTTGTG TTACGCGGCG GGTACCTCTA GAGGAATGGC 180 TTCACCCAGC AGGAGTAGGG TGGGGCGCGT CCACACTACA AATACGTGTC GAGGGTTTAT 240 CTGCGCCGTC CTTTCCTCTG TGAGGGGCGA GGTGGGGCGG GAATCCCTCA GCCAGCCCGA 300 CGAAAACTGC AGAGGCTTCT GGGCCTTTTA ACTTTGGAGA AGTTGAGGAC CTTGTCGCTC 360 ATTTGGCAGA AGGTGGGACC CGGATCTCAG TCCTGGCAGG AAGGGATGGC TCAGAACCTA 420 GGCGGAGTCA GGTCCGCTGT GGTCACGTCT CCGGTGACCC ACTTCCAGCT CTGGTCTTTA 480 CCTTGTACCG CCCACCTCAG GGCCTGGATG TAAAGGCACC GGTTCTCATT TCCTGCTGGT 540 TTTGTTTCAT TCATTAATTT AGAGACAAGG TCTCCCTGCA GCCTCGAACC CCTGGGCTCA 600 AGTGATCCTC CGCCCCAGCC TCTCCGTCCC GAGTAGCTGG GACAGCAGGC ACGTGCCACC 660 ACACCTGGCT GATTTTCAGA TTTTTTTAGA TCAGGTGTAG CTGTGTTGTC CAGGCTGGTC 720 TCAAACTCCA GCCACAAGCG ATCCTTCCAC CTCAGCTTCG AAAAGTATTG GGATTACAGT 780 AGTTAGCCAT CGTGCCTGGC CTTTTAAATT TTGGAACTTT AGGTTTACCT GAAAGTTGCA 840 GAGCTAGATC CCCCTAGTGT TAACATAAAC TCAGTACATT TGTCAAAACT AGGAAATTAA 900 CATTGGTATA ATACTATTAA TTGAACTACA CGCTTTATTA ATATTCTACC AGTTTTTCTG 960 CTAACGTTCA TTTTCTGTTC CAGGATCCCA ACCAGAATAT TGTATTGTAT TTTGCCTGTC 1020 TTGTTTTTAG CCAGTGTTGA GAGAAGGAGT CGCCTCTGTC ATTCCCTCCC CGACAAATAA 1080 TGACCTAACA ACTTTTTAAA ATCAAAGAAC TATTCAGTCT TTCAATTTAG TGAATATTTA 1140 TTGGTGGTCT GTTATGTCCT AGACACTGTT TTAGGCACTG GCGATTTAGC ATTAAACCAG 1200 ATAATCCTGC TGCCATGGGA GCTAAAAATA GCCCACACTT GTACCCACTG GTTGTCTTTT 1260 GCCATTTTGT ATTTCAGTTT TTGTTGGTTT GTTTGTTTTA AATGTAAGGG CATGCTGCTT 1320
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