Tag | Content |
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EnhancerAtlas ID | HS041-21323 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr9:34440610-34442080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Atoh1 | MA0461.2 | chr9:34442064-34442074 | AACATATGTT | + | 6.02 | Atoh1 | MA0461.2 | chr9:34442064-34442074 | AACATATGTT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 34441211 | 34441436 | chr9 | 34440757 | 34440835 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I034441 | chr9 | 34440999 | 34441198 |
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Enhancer Sequence | GGCCGAGGCG GGCGGATCAC GAGGTCAGGA GATCGAGACC ATCCTGGCTA ACACGGTGAA 60 ACCCCGTCTC TACTAAAAAT ACAAAAAATT AGCCGGGCAT GGTGGCGGGC GCCTGTAGTC 120 CCAGCTACTC GGGAGGCTGA GGCAGGAGAA TGGCATGAAC CCGGGAGGCG GAGCTTGCAA 180 GTGAGCCGAG ATCGCGCCAC TGCCCTCCAG CCTGGGCGAC AGAGTGAGAC TCGGTCTCAA 240 AAAAAAAAAA AAAAAATTTT TAAAGAAATG TTATCTTACT ATGTTGCCCA GGCTAGAGTG 300 CAGTGGCTAT TCACAGGCCT GATCGTATAG CACTTAGAGC CTTTAACTCC TGGGCTCAAG 360 TGATCCTCCT TGAGCCTCTC GAGTAGCTGG GACTCCAGGC TTAATGCCAC CACACCTGAC 420 TCTCACATAG GTTTTTAAAC TTGGCTGGAA AGAGAAAAGG ACCTAAGAGT TCTAGAATTG 480 CCTGCCCCAT CCCTTCCCCC AACCTCTCCC GGCTTGTAGC CCAGCTAAAC AGGAAACCAG 540 GTTTGGGTCC TTGCCAGAGC CCAGGCTGGG GCAGGAAGCT CAGGAAACAA GTAAGACCCT 600 CCTCAGCATA GAAGAAGGCT GCTAAGAAAT CTGTGGGAAG CAAAAATAAA CCCAGCCCTT 660 GCTGAACTCT CTCCCAGAGG AGGAAAAGAC CACAGTTGCT TCTACTCCCT AGTATGAGTC 720 AAGCATAGTC CTAGGAAGAT TCAGAGAGCA GATGCAGGAG CTTCATGAAG TGAGATACTG 780 CTGTTCCAGT GAGAACACAC TCAGTAAGGA CCCTCCTCTC AGAGAAGCAC AGGGCTTAGT 840 GAAGCAGGGT GGGATACATG TGGTCTGAAG ACACTCCAGG GCTATCTTGG GCTGATAAGG 900 AAGCAAATGA TGGTACAGGA TAAGAGCAGT GGTGGAAGAA GCAGACCTAA AGGAGAGAGG 960 GCCCGAGACC AGGTGATACC TGTGGGGGTA TGAAGGCAGA GAATTAACAG GGTTCTTTGC 1020 TGTACAAATG TGAAGGAAAT TCCTGATGGA ATAATGAATC AAGGCAATGA CAGTCAAGGG 1080 CTGTAAAAAC ATTAGGTGAA AGGCTGAAGG GGGCTTTTAT TTATTTTTTA TTTTTGAGAC 1140 AGGGTCTCGC TCTGTTACCC AGGCTGGAGT ACAGTGGCAC GATCATGGCT CACTGCAGCC 1200 TCGACCTCCT GGGCTCAAGC AATCCTCCTG CCTGCCAAGT AGCTAGGACT ACAGGTGCAT 1260 GCCACGATGC CTAATTTTTG TATTATTTTT GTATGGGGAT GGGGTCTCAC TATGTTGCCC 1320 AGACTGGTTT CGAACTCCTG GCCTCAAGTG ATCCTCCTGC CTTGGCCACC CAAAGTGCTG 1380 AATTACAGGC CACTATGCCT AGCCAACTTT TATAGTGGAG AGATCAGGCT AACTACACCA 1440 CAAAAAATAG GATAAACATA TGTTATGTGC 1470
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