Tag | Content |
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EnhancerAtlas ID | HS182-16811 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr4:5956900-5959030 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr4:5957894-5957907 | TTCTGGAACCTTC | + | 6.33 | JUN | MA0488.1 | chr4:5957208-5957221 | AAGATGATGTCAC | + | 6.2 | JUND(var.2) | MA0492.1 | chr4:5957207-5957222 | TAAGATGATGTCACA | + | 6.14 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH04I005955 | chr4 | 5957487 | 5958879 |
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Enhancer Sequence | CGGCACTTCC ATAGCTCTAA GCATGTCGCA GGGCCCTCCT TGAGCGCTTC ACAGATGCTA 60 ACCCACTCAC ACCTTACCAC GGCCCTTGGA GGCAGGCAAC CCCATTTTAC AGATGAAATC 120 ACCGAGGCGG GGAGAGGTGG GGTAAGGGGA AGAGCTGGGG TCCAAAGCCA GGCGGGGGTG 180 TGTGCTTGGC TCCTGGGTCA CCTGCCTCCA GCGTTACAGG GGAAAGGACG AGGGGTGGTC 240 ACACACCTGG GCTGTGAATG CCACCGCCGG GCACTGGCCA CGTGATACCT TTCAAGGCTC 300 CATGAGATAA GATGATGTCA CAGGGCTGTA ATTTCCATTT TCCCAGGAGA AAGCCAAGCC 360 TGAAGGGGTC TGGGCAGAGG GCCCACAGCT GCCGCGTGGT GGATGGGGAT AGGAACGCAG 420 GACCATATCA GCCTTCCTGG CTGAGCCCAA AGGCCACTTC TCAGCGCCTC ACCAGCCTCC 480 AAACTGCCCA GTGCTCTATC AGTCATCCCC GGCAGCCAGA TCCCAGCCTC CCAGCTGAGG 540 TCACTCCTGC TTGTGAGCAC CTGCAGATGG AAACGCAGCT GGCCCCTCCG GTGGAGTCAG 600 GAAGCAAACG CCTGCTTGCT AACTCCCACC TCCCCCACTC AGAAGCATCA TTGTCAGTGC 660 AGGGCCCTGT CTGTGATGCT AAATGGAATC CACACATCAC AGGCGGGTGC TGGCAGGGTT 720 GGGGGCCCCA GGCACCCCCA AGCTCTGCAA GTAGATTCAA AAACTGCTAC AACTTCAAAG 780 AGGGCGAGGA GTGGAGTTTG GCCAAGGCCA ACAAAATGAC AAATGTTAAC CTCCTCTGAC 840 CCAGGATTTC CTCTTAGCAA TTTACCCTCA GATACACAGT CACGCATATA ACCACGGGGA 900 TAGGTTGTGA GAAGTGTGTG GTTAGGTGAT TTCCTCATTG TGGGAACATC AGAAAGGGTC 960 ACACAGCAGG ATCACAAAAA AGGCAATGTC TTCCTTCTGG AACCTTCCAC TCCAGGATTA 1020 CAGAAAGCCA GGTATCTCTA CCACCATTTC CTACCCCAAC CCTACCTGGG CTTTTGCTCA 1080 TGATTTCTCC TAGCTTGGAG GCCTCCTCAC CCAGGCTGAT CCCTGCTCAT CTCCAAGGCT 1140 CAACTCAGAG GGCACTTCCT CCAGGAAGCC CTCCCTGACT GCTCATTGGT CAGCCGCCCA 1200 CTCCACGGCC CCTGGGCCTT GTGTTGTCCC TGTTCATGTC AGTCAGAGCA AACTCTGGAG 1260 GACAGGAACC TGGAGTGAGA CTCCTGTGAC CACACCCCAG CCCTTCACCT GTCCTGACAA 1320 GTGCTCGGAG AAGCATCTGC TGAGCAGAAC TCCTTTGCAG CTCAAGCAGA AGGCCTCCCG 1380 GGAGCACAGG AAAACAAGCC AGGCAGCAGG GAGGGACGTT GCACTAAAGC TTCTGCTGCT 1440 TGGCCTCAGG CCAAGCCAAC CCTCTCCTCT GATTTGCCTA AACGCCGAGG TGGGGCTCCT 1500 TTGTGCAGTG GCGGAGGGGT GCATTTACCT CGCAGGGTTT AGGGCTCCGC CTCCAGGGAA 1560 GTCCGCCATT GTTGTTTGCT GACAGTCCGT GTGACAAATT GTTTTCTGCT GCAGAGCCAG 1620 GCTGGACCGT CTGGCTGGTC TCCAGAGGCC TCAGGGTCAC TCGTAGTCAT TCCCTGCCTG 1680 TGGGGCAGCC TGAGACCAGC TCCTGTGTGC CAAGTTCCTG CCTGAACCTA CTGGGTTGCC 1740 AGAGCAGGTC CTGCCCCTGG AGCATCTGAT GGGTGGCAAG GAGCCACCAT GTGCCCTTCC 1800 AAATGCTGGG GTCTACAGAC CAGGCGAGGG GAGTCCGCCA TCCTGTACTG TGCCCCAGGG 1860 AGCCACGGCA CAAAGCTTGA GCCGACCCAA AGTGCTAGAC CCAGACGGCA ATTCATGGCC 1920 CGGGAGAATA AGTGGCTCTG CCTTGGAAAC ATGATTTATT AGGGAATCGT TGGGTTACGC 1980 TGCAAAGGTC GTCTTGGCTT GCTTTAATGG ATTTCCTGGG TTGCCTTTCT GCCCAGGCCC 2040 AGCACGTGAG CGCGGCAGAG GGGAGCATGA AGTCACAAGA CGACGGACGT CTGAGCTCCT 2100 GGGACTCCTG GAGACCAGAT GTGGTGGCAC 2130
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