Tag | Content |
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EnhancerAtlas ID | HS158-59009 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr9:131624430-131625580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr9:131625098-131625110 | GTTTGTTTGTTT | + | 6.32 | Nr2f6(var.2) | MA0728.1 | chr9:131625326-131625341 | TGAACTCCTGACCTC | - | 6.22 | Stat6 | MA0520.1 | chr9:131624881-131624896 | AGTTCTCAGGAAAGG | - | 7.24 | Zfx | MA0146.2 | chr9:131625349-131625363 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_26602 | chr9:131624602-131625184 | Esophagus | SE_65947 | chr9:131623859-131625082 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 131624638 | 131624918 | chr9 | 131624937 | 131625162 |
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| Number: 3 | ID | Chromosome | Start | End |
GH09I128862 | chr9 | 131624429 | 131625150 | GH09I128863 | chr9 | 131625481 | 131625497 | GH09I128864 | chr9 | 131625501 | 131626518 |
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Enhancer Sequence | TCAAGTGAAT TGAGCTAATT TTTGTATTTT TTGTAGAGAT GTGGTCTCAC TGTGTTGCCC 60 AGGCTTGTCT CAAACTCCTG GGCTCAAGGC ATCCTCCTGC CGCAGCGTCC CAGTGCTGGG 120 ATTACAAATG TGAGCCACTG TACTTGGCCA AGAATAATAT TAATAATACA ACCAGCTTTA 180 ATTTACTAGG ACTCACTCTG TCCCAATACT TTTGTCACTG GATCCTTTCA ACAACTCTGT 240 AAAGCAAGTG CTATCCTCAC CCTCATTAAC AGGTGAGGAA ATTCCTAACA TACTAAAATA 300 ACAACACTTA CATTGAGCTC CTGCAGGCCT TATAGCAGAT TGTACACCTG GTGCCAGCAC 360 AGGGCAGAAA CTCAGGAGAA ACAGATCCCA GCTGTGGCCC TCTTCTCTGC CCTGCCCCAG 420 CCTTGGCCCC TTGCCTTCTC TGGGCACTGC CAGTTCTCAG GAAAGGCGGT GCCTTCTGTG 480 TGTCCAGATC ACTGGCTCCA TGGGGGTCAA GAAGCTGGGT GGCACCTGTG CTGCACACGG 540 ATATGCTTAA ACAATCTTGC AGCCTTGGGG GTGGGGCTGG AAACCAGGAT CGGCTTCCAT 600 TGCAGGGGAC TGGCAGTGCA TCGGGCCTAT GTGTGGCCGG GTAAGACTGG GCATAGGAGT 660 CAATGTTGGT TTGTTTGTTT TTTGACACAG AGTCTCGCCC TATCTTTTTA TCACCCAGGA 720 TGGAGTGCAA TGGCATGATC TCGGCTCCCT GCAACCTCCG CCTCCCAGGT TCAAGTGATT 780 CTCATGCCTC AGCCTCCCGA GTGGCTGGGA TTACAGACGC GCGCTACCAT GCCCGGCTAA 840 TTTTTTTGTG TGTCTTTAGT AGAGATGGGG TTTCACCATG TTGGCCAGGA TGGTCTTGAA 900 CTCCTGACCT CATGATCCGC CCGCCTCGGC CTCCCAAAGT GCTGAGATTA CAGGCATGAG 960 CCACCATGCC CGGCCAGAAG TGAATGTTAT GTTGCACCCT CCACAGGGTA GGTCTGTTCT 1020 ATTACCACAC CCAGGATCAG GCCCCAAGTA GACACACAAG GAGGAGGGCA GTGCTGAGAG 1080 ACGGGGGAAG GATTAGAACA CAGGCTTTGA TGACCTTGGC AGTGTGACAT GAGGCAAGCC 1140 ATTTTACCTC 1150
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