Tag | Content |
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EnhancerAtlas ID | HS040-06921 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr11:68933680-68934500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr11:68934161-68934172 | GATGAGTCACT | - | 6.02 | JUND | MA0491.1 | chr11:68934161-68934172 | GATGAGTCACT | - | 6.32 | MEF2A | MA0052.3 | chr11:68934175-68934187 | TCTAAAAATAAA | + | 6.07 | MEF2C | MA0497.1 | chr11:68934173-68934188 | GTTCTAAAAATAAAA | + | 6.47 | Myod1 | MA0499.1 | chr11:68934071-68934084 | AGGGGCAGCTGCA | - | 6.22 | NFKB1 | MA0105.4 | chr11:68934239-68934252 | AGGGGGATCCCCA | + | 6 | ZEB1 | MA0103.3 | chr11:68934299-68934310 | CGCACCTGCCC | + | 6.02 |
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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 |
GH11I069166 | chr11 | 68933484 | 68934765 |
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Enhancer Sequence | CCATTCCCCC ACCAACGGGG CCACAGCCCC GGGAAAGGGG TGGCTCTTCT GGGTCCCCAG 60 ACTGCTCCCA GCTTTTCCTC TGTGGAGGCA GGTATGTGAG AAAGGATGCA GCCAGGCAGG 120 TGCAACACAC CTGGGCAGCC CGTGGCTGTG GCCATGGCCA TGGCCGGTCT GCATGTGGAG 180 GAAAAGATGG TGAGGTGAGA CCCTGAGAAA CAACTCTCTG ATCTCATCCA CCTCTCCCCT 240 CCTAGGCGGG ACGAGATGGA TGCACCCTCT GCCGCAGCCA CCTCTTCTGC AGGTGCCCGG 300 CTTCTCCAGA CTTGCTATTT TGGAGGGGCA GGTCAGTGGG AACGACCGAC TGCCTTGCAT 360 CTCAGCCACT CATGGGCCTC AGAGTGTGGG CAGGGGCAGC TGCAGCCCTC TCGAGCCTCT 420 CACTCCCTGC TTGGCCTCTG TAAGCCTGTC CGGGAGCAGC TCACAGAGCC CCTGTGGTGG 480 AGATGAGTCA CTTGTTCTAA AAATAAAAGA AGTGAAGTCA TGAAATAGTG TATTTCCTTT 540 TTAAGCCCGA TGTGCCTGCA GGGGGATCCC CAGCAGTGTG CTGGCGGCAG GGACCCTGAC 600 AAGGTCTGGA GCCTCAGAGC GCACCTGCCC CCACTTACAA GCCCCGGCCT CGGGGATTGG 660 GTGGAGTGTC CCCTGCCTCC AACGGCTCCC AGATGAGTGA GTAAAAGATG GCACGTAGAC 720 CAGGAGCGGG GGCTGACACC TGCAATCCCA GCACTTTGGG AGGCTGAGGT GGGAGGATCA 780 CTTGAGGCCA GGAGTTTGGG GCCACCCTGG GCAACATGGT 820
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