Tag | Content |
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EnhancerAtlas ID | HS040-02224 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:116810000-116811250 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr1:116811016-116811031 | TCTGCTGACTCATCT | - | 6.09 | REST | MA0138.2 | chr1:116811170-116811191 | AACAGCACCAGGGACAGAAAA | + | 6.18 | Stat6 | MA0520.1 | chr1:116810687-116810702 | GTGTTCCTGAGAAAT | + | 6.87 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_33703 | chr1:116808541-116812093 | H2171 | SE_66933 | chr1:116808541-116812093 | H2171 |
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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 |
GH01I116267 | chr1 | 116810481 | 116811570 |
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Enhancer Sequence | CAAGCATGAC AGTCAGTAAA CTTGTCTTCC CCTTATATAC CCAGTGGTAG CTGCATTTGC 60 AGTCTCCTGA CAGGGGAGAC TGTTCTCTTC CAAAGCAGAG TCCCCAGGCA GGAGCTACTG 120 TTGGCATAAA ACCATCTGTT GAATTGTACT GTTGTTGCAT GGAAGGCAAG AGGACTCCTA 180 ATGTTTGATG TCTTTGGGGC TTTTGCCTTG AAGGACAATG GGGATAGACC TTTGCCTCGG 240 AAAAGGAGCG ACTCAAGTAC AAGGCAGGTA AAACCATGGA AAGCAACAAA AGATCAGGGG 300 ACCCTTAGGC TGCTGTGAAG ACCGTACCAT GAAAATCGAG ATAAGGTGGT GCTTTCCTCA 360 GTCAGCAGGA GCACCCAGTC AAACAGAGCA CCTGGCCCCC GCCCAGCGAA TGAAGAGTGG 420 TTGATTCATG AAGAGCCTGG AATGGAGACA GCACCTGTCA GAAGAGGTGA TGGGGCATGA 480 GTATGTGTAC CAGGTTCAGA GTTCGGGCTC CTTCAGTCCA ACTGACCAAT AGGAGAAAAC 540 GCTGAAAAGA GACGGTGATT CAGGGCTGGC AGTGAGGAAG TCCCCAACTT TATCAATGTA 600 CCTGAATTAT TGTTTGGTTC TTCCTGTCTT TGGCTTTTGA TAGTTGTGGT CCTCAGCCAA 660 GAAGAGACAG AGGAAATGGA ACAGAGGGTG TTCCTGAGAA ATATGGGGGA GGAAGAAGTT 720 ATTGTCAACT GGCGCTCCCG CCTGCAATTA TTGTGGTGTT GGCGTTCCTC ATACTTCCCA 780 GTGCCGTCCC CACCACTCAT TGTGCTGGCT TGGAGGCACT CGGTTCAGAG TCTTCAAACC 840 CTCCTCCTCA GCCTTGGCCA GGCTGTCTGT CTCCTCAGGG CAGCCAAAGA AGATGAGCTC 900 ATTTCCAGAA CCCAAGAGGT GGCTCTGACC CTCTCTTCCC AGTTATTGCT GAAGTTGGGT 960 GGCTGAAACC AGTCAGGGCA TCATGCTGGC ACCAGGCCAG TCTTGCATCA GGCAAATCTG 1020 CTGACTCATC TCTCTCTTCT AAACAAGCTC TGAGAGTTGG CATGCAGGAA GCAGCACCAA 1080 GGAGTCTGAT GGCGTGGGCC ACCTGGCAGG GACTGACCAA GGGGAGGCGA GGAGCAGCAG 1140 CCACCTGCCA CCCCAATCCC ACATTCTTCT AACAGCACCA GGGACAGAAA ATATGTGCCT 1200 ACCCAAGAAT TTCAGGGCCA CAAGTAGAAA CAAGTATATC ATAACAGGGA 1250
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