Tag | Content |
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EnhancerAtlas ID | HS116-17579 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr2:8374310-8375440 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:8374687-8374705 | GAGAGGAAGGAAGGAAAC | + | 6.44 | Myod1 | MA0499.1 | chr2:8374598-8374611 | AGCAGCTGTTTCT | + | 6.28 |
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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: 2 | ID | Chromosome | Start | End |
GH02I008235 | chr2 | 8374410 | 8374864 | GH02I008234 | chr2 | 8374878 | 8375262 |
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Enhancer Sequence | TCGGCGTTGC CCTCTGAATA ATGGGACATG ACATTGACAC TTGCTTTCTC TATGTCAAAG 60 AATTCCTTGA GGATCAAACA CAGCTGGGCA CCAACGCACT GCATATGGTG TCAACAAATC 120 ACCTCTGTGT TATTATCATC AGCACACTCG CCCCAATCCT GGGGAACTAT TTCATGTCAA 180 TACTTCTCTC ACAAGAGGGA ATTTCTGTCC CGGAAACATG TCAGCCCTGA TGACACACAG 240 TCATATGGAA ATAGGAAGCT AACAAGCATT TCTCCTCTCT CCAGTCAAAG CAGCTGTTTC 300 TACACCCTTC TGCTTTTGCA CCTGCCCCCA GTGCTGTAAG TTCTATGGAA ATTCCACCCT 360 GGTGTCAGCT CCACACTGAG AGGAAGGAAG GAAACTCTTC CTCAGGTCCC TCTGACCACT 420 GTGGGAACCA GTGGTCATCA GGGTTGAAAT GTTTCCATGT TCAGGGGATG TAGGATGGTT 480 TTCTCTCCCT CTTCTTTTAT TGAAATAAGC TCTCAAGTCC TGTCATGAAA AGGTAAAGCT 540 TTCCTTTACA GGTAAAGTCC TGCAAGACAG GGCTTGAGAG CAGCACCATT TCTGAGGCTA 600 TTTATACACC CACAGTGCCC AAGGGTCAGG TGCGGCCATG AGCATAAAGC CAAACGACTG 660 AGCTCTGACA AGGCTGACTG ATCACTCTCC GCAGATTAGT TATTTTCAAG GCAAAGAAGT 720 GCAGGTGCAT GGCTTCCTGC AACTGAAATG ACTTGCCCAG TGAAGACAAT GCAGGCACAT 780 ACGTCGTGCT TCTCTGACAC AGCCAGTACA GTGCAGAGAA AGTCTCTAAC CACAAGCTGA 840 CCAGGCTGTG GCCTTGTGGC CCCGGAGTCC CAGTCTCCCT GCCAAAGCCC AGATTCATGG 900 ACCCCACGCA AAAAACAGGT GTGAGGCAGT GAGGGCGGTG AAATGGTCTC TATTGTTTTT 960 ATAATAATCT CTTCTCGTTT TCTATACGGC AGCTTTCATT CAGTCCATTA AATGCAATTT 1020 CCTGGCATCA CCCAAGCTTG AAAGGCCAGA TCAAAAGTAC AGAGTGTCCC AGCTGTGTGG 1080 TCCTCGTTCA GACCGAACAT TAACCACAGC CCTTGCAGAT GATTTATTCC 1130
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