Tag | Content |
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EnhancerAtlas ID | HS012-02149 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr11:7093180-7094570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HLTF | MA0109.1 | chr11:7093202-7093212 | ATATAAGGTT | - | 6.02 | HNF4G | MA0484.1 | chr11:7093952-7093967 | ACAGGTCAAAGTCCA | + | 6.68 | Hnf4a | MA0114.3 | chr11:7093953-7093969 | CAGGTCAAAGTCCACC | + | 7.19 | RARA(var.2) | MA0730.1 | chr11:7093943-7093960 | AGGTCATATACAGGTCA | + | 7.15 |
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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 |
GH11I007071 | chr11 | 7092784 | 7096055 |
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Enhancer Sequence | AGGATTAATT TCCTTTAAGG GAATATAAGG TTATTTGGGC TAGAGCTAGA AACAGATTCT 60 TTCATTTGGC AAGAGCGTGA CACAATAAAT TTTGTGTGTG TGTGTGAAAG ACTGTTCTGG 120 TTATTTATTG ATCGTGTAAC AAACTATCCC AAAACTTGGT GGCTTAAAAC AATAATGATT 180 TTATTAAATC TCATAACTTG GATTGGAATT CAGAAAGGGC CCAGCTGAGC ATTTCTTATA 240 CTCCACATGG TATTACTTGG GGTCCCTTGG TGGTATTCAC CTGGCAGCCA GATTGCTCTG 300 GAGGCCCCAG ATAACTTGGA CACGTCTGCT GCCTTGGCAG GGATGGCTGA AAGGCTGGGA 360 TGAGCCAGAC CCCTTTTCCT GTTATCAGCC GGAAGTCTAG TGATTCTCAG CAATTTTGAT 420 CCTTGCCCCC TCAGAGGAAA GAATTCAACT GAGAGGCAGA AGTAGGTTTA AAGCAGAGGC 480 AAAGTTTATT AAAGAAAGCA AAGTACACTT GGAAGAAATC AAGCAGGCCA CCTGAGAGAT 540 TCAAGTGTCT CTCTTGATCC TTGGTTTGAG ACTTTATACA TTGACTCATC TTCCAGGCTC 600 TTCTCCCCTG TTGATCCCTC CCTTGGGCGG GTTGTTGCTT GATTACCTGT GTGCAGTGGC 660 CTGTCACCAC TTGTGAGAGG CCCCGTGCAC GGTGTGTTTA CTGAAGTTGT ATGCATGCTC 720 CCTTGGGATG ATTTTTTCTT ACTGGTTGAG CTCCCCCAGA GGAAGGTCAT ATACAGGTCA 780 AAGTCCACCA TCTTGCTCCC CTTTGCACAC AGTTGAAACT TTATCAGGGA TTGTGGTTTG 840 CTGACTCCAG GTGTTTTCTA TCTGTTGGAG GAGTCCTTTC CTTCCTGGTG GCAGTTGTGG 900 CCACTTATTG TCTCAGAGAG ATAGTTTTAT GCTCACCTGT CCTTCACCTG ATGAGAGCCA 960 GACTTCTCTG GGGGCCCTCC CTTGTCCTGT TCATTATCTC AGAGGAAAAG GTTTACGAGT 1020 GCTTGACTAT GGCTCAAGAA TTGCTTGGCA TTCCTGGGGG CCCTCTCTCC TGCCCTGCTC 1080 TCATATCTGT CTAACTACCT ACTCTAACAT TGCTTGTAGT CTTAGGGCCT CTCCATGTGG 1140 TTTCTGCAGT GTGGGGATTC AGGATTTGAA AGGGCCAAGA GGAAGCTGCC ATTTATCTTA 1200 AAAGCTAGGC CCAGAACTGG CATAAAGTCA CTTCCATAAT CCTCCATTAG TGAAAATAGT 1260 ACAGGCCAGC TCAGATTCTG GGAGAATCAA TTGTTGATGG GAGTAGTGTC AAAGAATTTG 1320 TGGCCTTCCT TAGTTCACCA CAAACTTAAT GTTTTTCTCC TTGTCTGTGG GAGAAAATAA 1380 AGCCTTTTAA 1390
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