Tag | Content |
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EnhancerAtlas ID | HS007-02923 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr11:61484690-61486950 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr11:61486501-61486514 | GGGGACAGCTGCC | - | 6.29 | RREB1 | MA0073.1 | chr11:61486063-61486083 | CCACCCCCCACCCCCAAAGC | + | 6.62 | RREB1 | MA0073.1 | chr11:61486056-61486076 | CCACAGACCACCCCCCACCC | + | 7.54 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_23957 | chr11:61485459-61486314 | Colon_Crypt_2 | SE_25088 | chr11:61484277-61486685 | Colon_Crypt_3 | SE_63420 | chr11:61457154-61498627 | NCI-H69 |
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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 |
GH11I061715 | chr11 | 61483273 | 61487072 |
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Enhancer Sequence | AGGGGAACAG GCCCTTATTG TGATGGGCCG GGGTCTCTAG AGAAAGGGCA CCATTCAAGG 60 CCCTTAAAAA TAGCCCCAAG AGATGTATGA ATTGGCCTGG AGAGTGGTGC AGCCCACCCC 120 CAACCCTTAT GCAGCACAGG CCCTGCCACC CCCACCCCAG ACCTTGACTT GTTGGTGACC 180 AGCCGGAGAT TCCACCAGCC CAGGCGGGAG GGGTGGCTGG TCCAGCAAGG GGTTCCTTGC 240 ACTCCCTCCG CCTCGCCCGC CCCAGCTAAG ACAGCTAGAG CCTCTGCAGA CCTCTCATGT 300 GATTCTCACC AGGACTTTAG GAGGTAGGGA TAATCGACAT TTTACAAATC GACATTTTAC 360 AGTTGAGGAA ACTGAGGCAC GACTAATAAG TCACACAGTG GGTACGTGGT AGAGCCCAGG 420 TTCAAAACCA GCCAGCCTGG CACTTGTGTC CCAGCCTCTG TGCCTCGGAT TCTATGGTGG 480 TGGGCCGGCC ACTGGTGCAG GCCTGTCACT GGGTACCCAG CAGGGTCGGC CCCCAGGAGC 540 CCCGCCTCAT ACTCTAGGTA GGTACTGCTG TTGACCATGG CAATTGGCCT CAGGCTGGTC 600 ACCCTGAGGT GGGGGCAGTG GTTACCACTG GTCATATCCC TCCAGCGTCT TGACAGTCCT 660 TCAGCCACCT CACCTCTGCA GGGCCCAGGG CCAGGTTCGG CTCACTCCTT CCAGCCTGAG 720 AGCTGAAGCG AGCGGGCATT GTTCGGGCAG AGGAGGGGAG TGCAGAGTGA GTGTGTGTGT 780 TGGGTGGATG GTGTGTGATC TCGAGGAGTG TTAGCTATCC TGGGTTCCAT GGGTCCAAGG 840 GTGGGAGTGA GAGGAGGGAC CTCCCAGGGT GACTGAGAGG GGCCATCCAT GGGGTGGACC 900 TGAGAAGGAG ATATTCTTGG CTGCTGGCAG AGGCAGGCCT GGGGGCAGGC TGGGTAGGGC 960 CAGACCCTAG CCCTCCAGCC AGCCCCTCTG GGACAGCACT GCTCCCTCCT CCCCTGGTCT 1020 GGCCAGATCA GAGCAGGATG CGGCTCTACA GCACCTGCGG GGGCGTACTG CCCCCCCAGC 1080 CTCTAGATTC ATTCCATTTC ATTCTGTTCC ATTCATGTGA GGGGCTCCTG GCAGCCCCGA 1140 CAGCCCCCTG AGCCCGACCC AGCGCTGCAC CTTACCCTCT GTGAGCTACT TGGAGACAGG 1200 GAGGGGGCGG CAATACCAGC TGTTGGCAGC TCTGTTCTGC CCCAGCCCAA CTGCCACCCA 1260 CGGTGCCCCA GCCCCCCCTC CTGTCCTATC GTGTCCAACC CTAATCTGAA GCTGGTGCTG 1320 TCAGCCACAT GTCACAGGCA CTGCTGACGC CCCGGACCCC TGCAGTCCAC AGACCACCCC 1380 CCACCCCCAA AGCCCAGCCA CCCCACCACC ATGCTCCCTC ACTCTCCACC CTTCTCCCTG 1440 CCTCCCAGAA GCTGAGCTCC GACTCCTCCT TGGAGAGAGA GTGGGATGAT GTCACTTCCT 1500 GAGGGTGGGG GGAGGAGTAG GCACGACCCC GGCAGGCTAG CCCGCCAGCC CGCCAGGCCA 1560 CAGCTCGCCA AGTGGCTGCA CCGGGGATAG GGAGGCGGGC CGGGCGGACA TGCGGGCTGG 1620 CCACCTGGCC CCACGCCCTC TCGCCCACCC TGGGGGCTAT GCCCACTGGC CAAGGGAGAC 1680 TTGGCTGCTT CCTCCCCGAA TGATGCCGGG CTCCTCGGAC ACACATTTTC CCTGGAGCCG 1740 CCACTGGGGA GAGGAGGATC TGCCGCCTGC CCCGGACCAG GTGCCATGTA AGCCTCTACT 1800 GGCCCCCGGC GGGGGACAGC TGCCCACCAA CTTGGTCCCC AGCCCCCTGC AGCAGTTTAG 1860 TGCAGAGCTA CCCTGGAGCC CTTTATGGGT ATCTCTGGGG ACCTAGCTCC CTGTGGGGTC 1920 ACCTCCCACC CATGCTGCTT CCTTTCTCTT TGGGATGCTA AGGAGTGAGG GCCCTGAGTT 1980 CCTGGGCACT CTTTCCTGAG CTTGCTTGGG GCTGATTTGA ATTCAGCTAC TTCAGAGAGT 2040 TGAAAATCCA GCTGGAAAAG CTGCATGGCT CAGGGTGGGC TTGGGAGGTA TGGTTGCCAG 2100 GAGGGGTGTG ACCCTGCAGG GCTTACCCCA TCCTTCCAGC AGTGTGGGGT GGAAGGTGTC 2160 CCAAGCCCTA CTCCTGACCC TGCACCTCAA CCGTGCTCTT CCCTCCCTGG AGGCATAGCT 2220 GTGGTGGGGA CTTCTGTCTG ATGGGTTCAA AACCAAGTCA 2260
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