Tag | Content |
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EnhancerAtlas ID | HS012-15122 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr18:21002670-21003340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr18:21002823-21002836 | AGGGACAGCTGCT | - | 7.52 | TCF3 | MA0522.2 | chr18:21003207-21003217 | AACACCTGCT | + | 6.02 | TP53 | MA0106.3 | chr18:21003119-21003137 | AACATGCCAGGCCATGTC | + | 6.31 | TP53 | MA0106.3 | chr18:21003119-21003137 | AACATGCCAGGCCATGTC | - | 6.77 |
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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 |
GH18I023420 | chr18 | 21000838 | 21004105 |
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Enhancer Sequence | CCTCAGCCTC TTTTCTGTCA ACAACACATT CGGGGTCATG AAGCTCACCT GAGACACACA 60 GCCCCCAGCA TGCACAGTGC AGGGGCAGCA CAGGTCACAA ACACCCCTCC CCCCCCCAAT 120 GCAGAAAGCA CATCAGAATG CCAAATGAGT GAGAGGGACA GCTGCTTGCT CTAATTGCTT 180 TTTCATTTTA CTTGAGTCAT TCATAAATGT CAAAACCCTG TTTTTCATGA TAAATGACTT 240 GAGACACCAC ACCTCAGAAG TGACTATGAC CACAACCCAC CCATGTGTTG CGACACTACA 300 GTTGAGAACT CTGGCCTAAA GGACAAGTCA CTTGGGTGTG ACACATAAAG TCCTTCGGGA 360 CTTGCACCCG CCCCTCTCCA CGGTCAGCTC CTGTCTGTCT GCTATGTGCA GCCACATTCC 420 AGCCACAGCA GATGGCCCAC AGCCTTGGGA ACATGCCAGG CCATGTCATA CTTCTAGGAG 480 TCTGGTTGTG CCATCCTCTT GCCCCATAAT GTTCTTCCCA TCTCTTTGTC TGTAGTGAAC 540 ACCTGCTCAG CCTATAACAC CCAGTTTGCA CATATCCTGT GTGAAGTTTC ACTGACCCAG 600 CCAAGCAGAA CACACCAAAT GTGGGTCCTG CCTTCAAACA GTTTGGTCCA GTACAGTGAT 660 TCTCAACCAG 670
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