Tag | Content |
---|
EnhancerAtlas ID | HS040-28272 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr5:74832290-74833000 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX1 | MA0509.2 | chr5:74832318-74832334 | TGTTTCCATGGCAACA | - | 6.89 | RFX1 | MA0509.2 | chr5:74832318-74832334 | TGTTTCCATGGCAACA | + | 6.91 | RFX2 | MA0600.2 | chr5:74832318-74832334 | TGTTTCCATGGCAACA | + | 7.11 | RFX2 | MA0600.2 | chr5:74832318-74832334 | TGTTTCCATGGCAACA | - | 7.17 | RFX5 | MA0510.2 | chr5:74832318-74832334 | TGTTTCCATGGCAACA | + | 7.05 | RFX5 | MA0510.2 | chr5:74832318-74832334 | TGTTTCCATGGCAACA | - | 7.06 | RREB1 | MA0073.1 | chr5:74832417-74832437 | GTGGTGGGGGTGGGTGGAGG | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGTTGAATTG CCTGCTCTGC CATCTGGGTG TTTCCATGGC AACAGGAGGC TGTACCCCCG 60 GCAAATTCAG GCAGAAGCAG GACCACTGGG CCAGAAGCTC TAGCAGGCAT GGCTCACCTG 120 GCTACCAGTG GTGGGGGTGG GTGGAGGCAC CCACCCTGCC CCCTGGGTGT TTGCTGGGAC 180 AATAGTAGGC TGTGCCTACC AGCTGAGTTG CCATAGAAGC AGGACCCCTG GGCCGGAAGC 240 TCTAGCATGT GTTGCCCCCC AGCTACCAGA GGCAGGGATG GGCAGGGTGA CATGCTGTCT 300 TGTCTGGGTG TTTACTGGGA CAACAGGAAG CTGAGCCCTC CTGCTGAGTT CACACAGATG 360 TGGAGCTGCT GGGCTGGAAG CTCTCACAAG CATTGCTTGC CTGGCTACCA GTGACGGGGG 420 CGGGTAGGGT CATGTAGTTT GCTGTCCCAG CATTTCTTGG GATGACAGAA AGCTGCATCC 480 TTCAGCTGAG TTCACACAGA AGCAGGACTG CTGGGCTAGA AGCTCTAGCA AGCATTGTCT 540 GCCTGGCTAC CTGTGGCAAG GGTAGATGGA GTGGCCAGCC AAATTCTGGC TGAAGCAGGA 600 CCACTGGGCT GGAGGCTGTT GCTGAGCCCC ATCCAGCAAG GAGTAGTGGA GAAATCTTAC 660 TGCTTTCAGG CACTGCAGTG GCGGCCTCTA TTGAGGCTAT AACACTGGTG 710
|
| |
|
|
|