Tag | Content |
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EnhancerAtlas ID | HS101-02337 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:114217220-114218350 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr1:114217998-114218009 | GGATGACTCAG | + | 6.32 | JUN(var.2) | MA0489.1 | chr1:114217995-114218009 | AAAGGATGACTCAG | + | 6.18 | JUNB | MA0490.1 | chr1:114217998-114218009 | GGATGACTCAG | + | 6.14 | TCF7L2 | MA0523.1 | chr1:114217463-114217477 | CAAGTTCAAAGGGA | + | 6.03 |
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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 | AATTCAATTA GAAAGGCAAA TGATCCTGGT AATTATTAGA TGGTATATTC TAGTAATTAT 60 TAGAAAAGGT GCTTCTGGGT GATTGCAGTT TTGAATTTTT CATTTCACTC CCATTAGTCA 120 TTTCATAAAC ACATATTGAG TGTTTGCATT ACCCAAAGCT TTATGCATGC TACTGAATGA 180 GTTGGGAGAG TGACTCAAAA CAAATAAGAT ATTATCCTCC CTCAAAATGA CCAGACACAT 240 GCACAAGTTC AAAGGGATGA ATAGAGAAGA TTTCACAGAA TAGGTGGCAT TGACAGGTGC 300 ATAGGATTTC AATAGGGAGA AATTAAGGAG AGAAAACATT CCAGGCTGAA TAAATGAGCA 360 ATGGCGTAAA ACTAAGGAAG TATAAGTCAT GTACAGGGAA CTTCAAATGG TTGAGTTTAC 420 TTAGATTTTA TTTAGAAAAT GCGTAGATGA ATAGAGGAAA TGAGAATATA AAAGCCGATG 480 GGTCGCAGGC ATAAAGGTCC TAGGCAGTGG GAAGCCATGG GAGGCTTTTT AGCCAGGAGT 540 TTCCCCTCAG AGCAATCTGC TGATAAAAAT CTGTTAGTGG TGTGCAGGAA GGATGAAGGG 600 ACTCCAGGTA GCTGTAATTT ATGCATACAG TGGTAGTGGT GGGAGTATAA CTTGAATGGT 660 AACGCTTTGG ATGGAAGATA AGAGATGCAT ATAAGTTCAA ATTTCAGTGA ATAAAGGACC 720 AGACTAGATG AACAACAAGT ATCCTTTAAA TGAGGGATGA AGGAAAAGGA AGAGTAAAGG 780 ATGACTCAGA AGCCTTGCCC CATCTGTACT ACGAAAACCA TCAGGGAAGC CAAGGGGAGA 840 AAGGATATGG CAAAGACTGA TGGTGTAGTA AGTTGGAGTC ATGTTGAGGT GAAGGGAACA 900 GCTAGTAGAG CAGGTGTAAA TGTTTAGCAG GCAATTACTA CTAGTAGTGG TAGAAGCCCA 960 GATTGCGACA TTACTGAGAA GTGATGATTG AAACCTTTGT GGTAGATAAG ATCACTAAGG 1020 AAGAATATTT AGAGAGTACT TAGCCAAGGG CAGAGCTCTG AGCAAGGCAT GTAATTAGTG 1080 GACTAGATAA AATAAAGAAA ATGGGAAGGC GCAGCATGCA GAGCCACAGA 1130
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