Tag | Content |
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EnhancerAtlas ID | HS012-25969 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr9:38226490-38227630 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr9:38226513-38226528 | TGAACTCCTGACCTC | - | 6.22 | RREB1 | MA0073.1 | chr9:38227460-38227480 | AGGCTGGGGGTGGTGTGGGG | - | 7.5 | SP2 | MA0516.2 | chr9:38226895-38226912 | AAGGGGGCGGGGGCTGG | - | 6.06 | ZNF263 | MA0528.1 | chr9:38227048-38227069 | AATGGAGCGGGGGGGGGGGGG | + | 6 | ZNF740 | MA0753.2 | chr9:38227056-38227069 | GGGGGGGGGGGGG | - | 6.03 | ZNF740 | MA0753.2 | chr9:38227057-38227070 | GGGGGGGGGGGGG | - | 6.03 | ZNF740 | MA0753.2 | chr9:38227058-38227071 | GGGGGGGGGGGGG | - | 6.03 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_33966 | chr9:38226496-38227139 | HCC1954 | SE_33966 | chr9:38227167-38228604 | HCC1954 |
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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 |
GH09I038226 | chr9 | 38226485 | 38229029 |
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Enhancer Sequence | TCACCATGTT GGCCAGGCTG GTCTGAACTC CTGACCTCAG GCGATCCGCC CACCTCGGCC 60 TCCCAGAGTT CTGAGATTAC AGGCGTGAGC CACCGCGCCC GGCCCAATGA GATAATATCT 120 GTAAAACATT CAGAACAAAG GACACTGAGT ATCCACTGGA TTTGGCAGTT AGCAGTGCAT 180 CAGAGAGATG TGGAGAGAGC TGCTTTAGAG GAAGCAGAAG CCAAAGTGCA GGGATGGGGA 240 AGTGAGTGAC TGGAAGGGAT GAGAAAGGGG AGTGGAGACA GCCCCCTGAG AGCTATTGGG 300 CGCAACAAGA GAGAGGGTAG TTTGATGGAG AGGGCGTTAT TGACAGGAAG GTGCCAGTAG 360 GATGGGAGTG ACTGCAGATA CAGGAGAGAC GAAGGAGAAC AGAGTAAGGG GGCGGGGGCT 420 GGACTGCCTG CATCCAGGTG CAAGGGGAGG TGAGGGGGGG GTCGGCAGGG AGGGAGGGGG 480 CTCGTTCATA CCTGCTGCCG GGGTGCTCTG TATCCTCAAG TGGAGCAAAC TCATCTGTGG 540 AGGGAGAGAA GAGTGGCGAA TGGAGCGGGG GGGGGGGGGG GCTCCGGGAG GGCGGGGGAA 600 GTGTGAAGTA GCTCTTAAGT GGAGTGGGGG AGGGTTAGAA AAGACGGTGA CAGGCGGTGC 660 TAAGCAGAGA CCAGAATCTG GAAGGGTGCC AGGTTGTGGG TGTGGGGGAG GGGGCTGTTC 720 CGCCGCAGCT GCAGCTACAG CCAGGAGGTG AGGGTGAGGA AGCTGGAGGG AGGCATGACT 780 TTTGGAGTGG GCGGGCTCAC CGGGAGGATG ACCAACTAGA TGGTCCAGAT TGCCTGGAAA 840 TGGAAAGTCC CTCATCCCAG GAATGCCTGA GGCCAAACAA ACCAGTAGAG TTGGTCACCT 900 ACTGCAGAGT GATGAAACCC TGGCCCCCAC GGGGGTGAGC GTGCTGGCTT TGTGATCGGC 960 GCTAGGATGC AGGCTGGGGG TGGTGTGGGG GTGTAAGGGT AGCCTGGACA CTCAGGAAAT 1020 AGGACTGGGG GGTTGGGAGG GAGGTTAAGG ACCTAAGGGT GTCACTCACC TGTCTTCCTG 1080 GTTCCTGAAT AGTGCCTGGC CTTCCACCAG GCACTAAATA TTTTTCCAGA GACTGTGAAA 1140
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