Tag | Content |
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EnhancerAtlas ID | HS073-13695 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr8:6634890-6636530 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr8:6635706-6635719 | TTCCAGAACTTTC | + | 6.29 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr8 | 6635170 | 6635366 | chr8 | 6635390 | 6635806 | chr8 | 6636412 | 6636507 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I006777 | chr8 | 6635073 | 6637390 |
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Enhancer Sequence | GAATGAGTGA TGTATTGGAT GCATTTGTTA TTATTTTACT CTATGAACTA TAAAGAAAGA 60 TTGATGACAC CTAAACTCTT GGGCAGGATC CCCTTTTCCT TGCTCTGTAA TGCACTTCCC 120 CTGGCAAACT CCTACTCACT TCTCAAAACC CAACCCGAGG GTTTGTCTTT CTGAAGGCTA 180 CGCTGTCTCC ACAAGCTGAG CTGATCAGCC CATCCTTAGA ACAATCACTT GTTAAACCCA 240 ATGACAAGGG TGTGATGGGC TATGTGTGTC CCACCCCTAA TTCACACATT GAAGCCCTCA 300 CCCCTAATGT GATGGGATTT GGAGGCGGGT CCTTTGGGAG GTGATTAGGT TTAGATGAGG 360 TTGTGAAGGT GGTGTACGAA GCCATTCTTC ACTGTTCTAA AGAAATACCT GAGATTGGGT 420 AATTTATAAA GAAACGAGGT TGGCTTGGCT CATTGTCCTG CAGGCTGAGC AAACATAGCG 480 CTTGCCTGTG CTCAGTTTCT GGGGAGGTCT CAAGGAGCTT TTACTCATGG TGGAAGGTGA 540 AGTGAGAACA GGCACGTCAC ATGGTGAAAG CAGAAGCAAG AGAGAAGGAG GAGGTGCCAC 600 ACACTTTTCA CAACCGGATC TCGCAAGTAC CTGCTCACTA TGCAAGGTCA GCACCAAATC 660 ATGAGGGATC TGTCCCTATG GCCCCCACAC CTCCCACCAG GCCCCACCTC CAACACTGGG 720 CATCACAATT CAACATGAGA CTTAGAGGGG GCAACATACA AACTGTATCA GGTGGAGCCG 780 CATGACGGGA CTAGTGCCCT CAGGAAGAGG AAGAGATTCC AGAACTTTCT CTCTGTGTCA 840 CTTGAGGACA CGGCCGGAAG GCAGCCCTGC CTGGACCTTG AAGCTGGACT TCCAGCCTCC 900 AGAACTGTGA GACATAAACG TCTGCCGTTG AAGGGGCTCA GCTTGTGGTG TGGGATTGTG 960 GTAGCCCTAG TGAGGCACTG GCCTGTTAGA TGGAAACTTC TGGAGCTAAG GGGCTTTCAC 1020 CTTTGCACCC AGCACCTGGT CAGAGCTTGG ACATCCTCTC CTAAAGATTT CCCTAAGCTT 1080 GGGTTAAATT AATGAGCTGC CCAGATGCCA CAGACCATGT CTGAGAGCCT GAAGCAGCTG 1140 AGGAGGTTGT GTTATTTAAG TTGGGGCTTG ATTGTTTCAG TTCATTTTAC TCTAGAGGCA 1200 GGAAAAACAA TAACGGGTAA GGCCTCTCAC CCCGATGTTT TAGGGAGTGA GGCAAAGCAA 1260 CCACCCCTGA CTTGACAAGA AGACCATTCT CAAAGGTGAT CAAAATAGAC TCAGGGAAGC 1320 AGGCCTGTGG TTCCTTGACG CTCCTCCCAG GCCTTCCTGT TTGTCCCAGC CACCAGCATC 1380 CTGCAGGTAC CGAGAGGGTG GATGTGGACT CACTGCTCGC AGGCCGCCAG CCTGCTAGCC 1440 CAGTGTCCCA AGTCAAAAGT CACAGCGACA TGCCGGAAAG ACAGTTTCCA CAGGACGAGT 1500 GGAAAAGGGG GCGTCTCTTC TGCCCATCGA AGGGTGCATC CACCTGTGGT ATTAAAGGAT 1560 TTACAACTGG CCTCAGAAAC GCTGCCGGAG CTGCTCCTTG GGGTCTGTCC GATGGGAAGA 1620 GGCCCCTCCT GTGGCTCCCC 1640
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