Tag | Content |
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EnhancerAtlas ID | HS042-09206 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr11:123669980-123671140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BHLHE40 | MA0464.2 | chr11:123670420-123670430 | ATCACGTGAC | + | 6.02 | TFEB | MA0692.1 | chr11:123670420-123670430 | ATCACGTGAC | + | 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 |
GH11I123799 | chr11 | 123669769 | 123672894 |
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Enhancer Sequence | AAGCATTGTC CTAGGATTAG ATGAGGCCCT GATGTCATAG ACAACAACAG TCACCTCATT 60 GTATAATTGA GGCAACTGAG AAAAAGAAAT TTTTTGACTT CCATGAAGCT ATTGTTTTAA 120 TTTGTGGGTA GACCGTGATT GGAACCCAGA ACACCTGATT CCCATTCAAA GGCTTGCTCT 180 CTAAACCACA GCGCAGCTTG TCATTTCCAG GCTTCCCAGG ATTAAGCTCT GGTCAGATTT 240 TTACTTCTCT AGTCTGCATC AGTTTGGCAT CAGCCTCAGC TGTTTCTGTC AGCTGCTCTT 300 ATTTCTGTCA ATCTCTGTGA TGGTCCATAT GTAGGAACAG CTGTATGCTC CTCCTGCCAG 360 AGCTCTCTCT GGCACTGTGC AGTTGCAGTA TGTTCTCATG CATGAAGAAT AGTATGAACA 420 GTTATACTGT CTGTCAATAC ATCACGTGAC TCAGGCGCCA GTGGCAAATT TGTGTCGCCT 480 GTGCCTCAAT AATATTCACA GACATGAGAA TACTTTTATA AGTTTAGAGA ATTGTGTCAT 540 GCATAACCTC CTGTCACATC TGATATAGGA GAATTTTTGT TTTTCAATTT ACTAAAAATT 600 ATTCTTCATT AAATGAAATT TTAGTCTTTT GAGTCTGCGA AACCGACTGT CTGTAATCAG 660 GACCCTTCTA GGTTGGAAGT TGGAAAGAAA TTGCTATGTG AGTTATTGAA TTTTGCAAAT 720 GTCAACCATA TTACACTCTA TCTCTAAAGT ATTCAACACT AAATTCTTAT TATCCAGGGA 780 CAGTTTGTAA ATAATAGAAA GTATAATTGC TCAAGTTTGC TGAATACACT TCTCTCAAAA 840 GTTTAAGGTT TGTCTCTAAG GTGGAAATCA ACAGAAAGAC AGATGGCTGA GACCAGTGAT 900 ACTACATTCT CAATATTGTG ACCAGCTGTC TACAGCAGCT GTAGCCGCTC CCACAAATCC 960 CTTGAGGATA AGAGCAAGAA AAGGCGTGCT CTTTGTTACT GGCCTTGGAG GACAACCTCA 1020 ATGTGTGCCC TTGATGGGCT GAGTTGAATG ATGCGAAACA TACCAAGACT TTGATTGCAT 1080 GTTAGAGAAG GTAGATCCAT GACTGAAAGT AGCTCAGGTT CACCCTGTAT TGACTTCCCC 1140 AGTGGCATAA AGAAGCATGG 1160
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