Tag | Content |
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EnhancerAtlas ID | HS150-02190 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr11:44467210-44468520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr11:44467213-44467231 | GGAAAGAAAGAAGGAAGT | + | 6.9 | FOS | MA0476.1 | chr11:44467556-44467567 | GATGAGTCACA | - | 6.14 | JUND | MA0491.1 | chr11:44467556-44467567 | GATGAGTCACA | - | 6.14 | MYCN | MA0104.4 | chr11:44467814-44467826 | GGCCACGTGGTG | + | 6.07 | MYCN | MA0104.4 | chr11:44467814-44467826 | GGCCACGTGGTG | - | 6.07 | Nr5a2 | MA0505.1 | chr11:44467853-44467868 | ACTGGCCTTGAATTC | - | 6.41 |
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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 |
GH11I044445 | chr11 | 44467501 | 44467650 |
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Enhancer Sequence | GGAGGAAAGA AAGAAGGAAG TTTGCGTTTT GTTGGTAGAG CTGATCATGC ATATATGGAG 60 TGCACAGGAC GAAGCATCCT CCTTGTCATT AGAACCGTAA GACATCCTTA TGTGGTGGAT 120 GCAAATGTCC ACATTTCATC GGGGGGACAC TGAGGCTCAT AAGACCAGTG AAGGGGCCCA 180 ACAGGGAGGG GATATGTGCA GCATGAATCC AATTAGTTTG TCTTCCCCTG GATCTGCCCC 240 AAGCCTGGGA ATCATAAGAG GCTTTGGAGA GCACCTGAAA TTAGCGTGGA CCTGGCAGGA 300 GTGTTCTGCC CCTCAACCTC CCTTTGTGCA CCCCACATAG CTGGAGGATG AGTCACACAC 360 CCTGGAGGAC TTTCCTAATT ATACAGGTAT GTAGCGGCTT CTGGCCAGCC TCCTGGAGTT 420 AGAGAAGGGG CTACCTGCTT GTTCAGGCAG CAGGGTGCTT GAGAGTATGG CTGACTTTGT 480 GTCACCTGCC CTGGGATCCC CAGGATTCTA TTTGTCAGAG CAGGGATGAA CGAACCAAGG 540 CCCAAGGCGT GAGACTAGAT TGTATCTAGT GGGGCTGTCA GAGCAAGCCA GGGCACTTCC 600 CTGGGGCCAC GTGGTGGAAT GGTCAGCTGA GGACACAGAT AGAACTGGCC TTGAATTCCA 660 GTTCTGCCAT TTAGCAGTGA TCTTGGCAAA CTCACTTACC CTCACGGAAC CTCGACTGCT 720 TCTTCTGAGA ATAGGGGAAA TGATGGTGCA CCCTCCAGAG AGGTGCCAGA GGACCCCGAA 780 TGTGATCACG TTTGTATGCT AGGTAATGGG CTCAACACGT GGTGAACACT CAGTGTTGGT 840 TGTTATGGTA ATGTGGATGC TATTGTTGTC ATCCCTGGCC CATTACCAGA ATCTTCTACC 900 AGCTCAAAGC CACACACTGG AGGTAGTGCC GGAGCTGGTT TGCTAAGTCA TTGAGGCATG 960 TGACTGCACA TGGGGGGTCC CTGATGGTCT ATTTTCACCA GCACCCGTCC TTATCTGGAG 1020 CCTTGAAGGA TTTTTGGCAT TCAGAGAGTC CCCCCTGGAG ATGTCTGTGC CTGCGAAGAG 1080 GGGCTGATTG ATGGGGTGAG GACTTCCACT GGGGGCAGCT GGGGTGGCAG TGCAGGCCAG 1140 TGAGACCCCC TTCCTCTCTG GGTCTGGGCC TCTTTTTTCT ATCAGCCTGG CAGATTCTGG 1200 AACGCCTGGT GCCCTCTCAG CAGAAGCCCT GGGGTAGGGT TTCTGGTTGG GTTTCAAGGG 1260 CTGCTCAGAG GTTGTGGCCA TCTTTGCCGC TGAGCTGTGG TGCCGCTTGG 1310
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