Tag | Content |
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EnhancerAtlas ID | HS184-31821 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr9:137191500-137192500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MITF | MA0620.2 | chr9:137191955-137191973 | CCAGATCACATGACCTGA | + | 6.04 | MITF | MA0620.2 | chr9:137191955-137191973 | CCAGATCACATGACCTGA | - | 6.04 |
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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 |
GH09I134299 | chr9 | 137191781 | 137191930 |
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Enhancer Sequence | TTCCCAAAGA TTGTGGTGGA AGCTGTGTTG ATGGGTGTTC TAACCGGTTC ATCTGAATTC 60 CTCGAATGTG GATTCCAATC CTTCATCTCA CATGTGCCAT AGGTTTGCAT TCGAGTATAT 120 ACAAGTTATC AATTGATGAA TAAGAAGTTA TCCCCCAACA CGTAGTGGCT GTAATAAAAC 180 CAACAATAAC CATTTATAAT CTTCCACAGT TTCTATAGGT CAGGAACTGG GGAGCAGCTT 240 AGCTGGGCAG ATCTAGCTTG GAGTTTCTCG AGAGGCTGCA GTCAACATAT TGGCTGGGCT 300 AACAGGACTT GATGGAACTG GAAGATCCAG TTCCAAGGGG CTCACCCGCA TCTCTGGCAG 360 ACTGGTGCTG GCTGTTGGCA GGAGTCACCA GTTCCTCCCC GTGTGGACCT CTCCACAGAG 420 CTGCTTGAGT GTCCTTACAT GGCAGCCAGC TTCCCCCAGA TCACATGACC TGAGAGAGGG 480 CAAGGCAGAA GCCATGAGGT CTTTTATGAC CTAGCTTCAG AAGACACACA AGGCATTTCC 540 ACAGCGTGCT ATTGGTTACA CAGGTTGCGG GGCCATCCAT GGGCACGAAC ACCAGGAGGT 600 GGGGATCACT GGGGGCCATC TCGGCATCTG CCTACTACAA GCATGAACTT ATTAAGTTTA 660 CATTTAAAGA TAAACTCTTT CTGGAGTCGG TGAGTGCAAA CTCTCAAGCC TTTGCTGTTG 720 CTGTTTTTAG TTCTTCCAAA TAAATTGATG ATAATTCCCG GTGATTGCCC ACACTGCACC 780 AAATCTTGTG GGCATCTGTC TGCCCAAGGC AGTATTTTAA AAGCTGCCTA ACACTGTCTC 840 TTTAGCAGGC GGGGAAGCTG ACAAACCTGG GTACTGAAGG CAAAAATGTC CCCACGCACA 900 ACCTGTCCCT CCCACAACGG CTCACACAGG ACAATAAAGA TGGAAGCAGA TTGTGGCACT 960 GGTGCTCGTG GGATGGTCAA TGCCATCATA ATCAACAGTG 1000
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