Tag | Content |
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EnhancerAtlas ID | HS092-15322 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:111463290-111465400 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr13:111463539-111463550 | AATGACCTTGA | - | 6.32 | Esrra | MA0592.2 | chr13:111463540-111463551 | ATGACCTTGAC | - | 6.32 | Esrrg | MA0643.1 | chr13:111463540-111463550 | ATGACCTTGA | - | 6.02 | FOXA1 | MA0148.4 | chr13:111464277-111464293 | GGATGTTTACTTAGTG | - | 6.17 | FOXC1 | MA0032.2 | chr13:111464279-111464290 | ATGTTTACTTA | - | 6.02 | Foxa2 | MA0047.2 | chr13:111464280-111464292 | TGTTTACTTAGT | + | 6.44 | SPIB | MA0081.2 | chr13:111464184-111464196 | GATGCGGAAGTG | + | 6.74 |
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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 | CCTCCCAGCT GGGTGCTCCA GCCCCAATAG CGTCGCGATG CTGGGGACGA GGTCTAGGAG 60 AAGGGAAATG GGGGGCACTT AGAGCCCCAA ATCCATGAAC CACGCTGGTC TGTTTTAGGA 120 AAGCAACATC TTGAGGCTTC ATGGTGTTCT GTGCTCCCTG CTGGGAAGCG CTGGGCTGGC 180 TGGAGGTTTT CATCTCGGGA CTGGGGGTGC ATCCCCACAC TGCCTGGCTG AATATGTTGG 240 TGCTTTCCCA ATGACCTTGA CGTCTGGTGT TTGTCTGGTG CAATACGTCA GTGGGGAGAC 300 GGTCGTGCTA ACAGCGTATT CGGCTCAGCA AAAGCTTTCA TTGCATGCAT CCATGGCCTC 360 TTTGCAAAGA TGGGAACAGC ACGTCTCAAT AACACACAAT TTCATCTGGC TCTGATGATT 420 CAGAAGGCGC CCCGGTGCCT CAGGCTCATC ATTAGAAGCC AATGATGGCT CTGTAGATGT 480 GGTAGTAAAG TCCAGGTAGC CGAAAGATTG AGTAAGGAAG CATTTGCTGG GAAATGGGGG 540 TCTCTTGCCG CAGTGCTCCC CAGACACCTC AGGAAGTGAC CTTCTGCCTG GGGCCTCTCT 600 CCGCTGACAA TAATGTCACA CACTTCCTTG TCTCAAAGTT GAACACTGCC AGAATGATCC 660 ACATCCAAGG TAAGCTGGCT TCAGCTTGTT AATTTAGTCC TGCTCTCAAA GAAAAGGAAG 720 AGGTCCTCAC CCTGGCTGAC ACCTCTGGCC GCAGTGGCCC TGGTCCCCAG GGTGACAAGG 780 GCCACACTCC TTAAAGAGCC TGAAATTCCC AGGAAGCTCC CCTTTTAAAT CCAGTTAGGG 840 AATATTATTT ATAACACACG CCTCACAGAT ATTAATTCAT TAAGAGAAAT AATGGATGCG 900 GAAGTGCTGA GGACTGAGAG TAACCTGCTA ACACGGCCCC ATCCTCAAGG GGCTTTCCCC 960 ATTTAGCCGG GGCCTGAGAA CTGTGTAGGA TGTTTACTTA GTGCTTTGAA AGAACTCACT 1020 GCATCCCCTC AACAATCCTT TCATGTGGCT GTTATAATTT TCTCCATGGT TGCAGATGAA 1080 AAAAAAAATC ATTCGGGAAG GTTGAGCCAT TATCCATGGC CACAGAGCTC CAAAGCGGTG 1140 GAACTCGGAA TTGAAGCCCA GGTCGGTTGA AGCCAGGGCC GCAAACGTGC TCCCTGCCGC 1200 CCCACTGCCT GGCCGACACA CTCACGGGTG CCGGGGCCAC TGCACGCATG ACAGTGCCAG 1260 GAGCGTGCAC TTACTCCCCG AGCCCTTCCC TCCACGGCCA GGCCCGCAGT GTGAGTGCCA 1320 GGGCCTTCGG CGAAGCCCAG GGAAGCCCAG CGCCCTCGCC CTGGTCCTTT GACACATGAC 1380 GAGACCTCCT CTGGGCAGAG GCCCCTGGAT TCTGGGGCTT TCTGCCAGGC AGGGGCTGGG 1440 GCAGGCCCCG CACGCAAGCA CCTGCCCCCG CACACAGGCA TCTGCGACCC CGGGACTTAG 1500 CCCCCGCTGG CCCGCTGCAG TCTCCATTCC TTAAGCGCCC AGAGCTCCCT CTGCGCTCTC 1560 CTGTGCCCGC GTCTCCTCTG TTCTGTTTCG TTCCGCTCTG CTTCGGGCTT GTCTCAATTA 1620 CATTTCCGTA AGGGTTCGGG TCCTCGGCTT ACTAAGGGGC CTCTGAGAGG CCAGCTGGCC 1680 ACCGGGACTG TCTTTCCTGC AGTGGAACTT TCCAGATTAT CTTCCTTTCC CCCATCTCGC 1740 CTTCTGCCTC CTGCCGTCTT CTCGGTGTTT AGCTCGGGCA GGGTCCCTCC TGCAGAAACC 1800 GCTCCTGCCC GCAGCGCGCG CGCTTGCTGC CTCCCGCCCG GCTAAGGGAG GGCGGTTTCA 1860 GACAGATCCA CTGGAGGGCA GATCTCCAGA GCCGGGAGCC AAAGGGGGCT GTGGCAGAAG 1920 GGGAGGCGGC CTTCGGGCTC AGGCGAGACA GGCTGACTCC CCCAGGAGGA CCGCGCTGCC 1980 TGGGGGAGGC GAATGCAGGG CCCATGAGGC ACTGACAGGA AGAGCCCCTG ACGGCGGGGG 2040 GCAGCTGAGG AGCGGGAGCT CCAGGGGGAG GGGGCAGAGA CTCGCCTCAC AGCGCGCCCC 2100 TCACGACGTC 2110
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