Tag | Content |
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EnhancerAtlas ID | HS091-07684 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:61393580-61396310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr11:61394345-61394357 | TCTATTTATAGT | - | 6.22 | MEF2B | MA0660.1 | chr11:61394345-61394357 | TCTATTTATAGT | - | 6.37 |
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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 |
GH11I061625 | chr11 | 61393045 | 61396713 |
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Enhancer Sequence | CTCAGCTCAC TGCAACCTCC GCCTCCCAGG TTCAAGCGAT TCTTTTGCCT CAGCCTCCCG 60 AGTAGCTGGG ATTAGAGGTG TGCACCACCA CGCCCAGCTA ATTTTTGTAT TTTTAGTAAA 120 GACAGGGTTT CACCATGTTA GCCAGGCTGG TCTCGAACCC CTGACCTCAA GTGACCACCT 180 GCCTCAACCT CCCCAAGTGC TGGGATTATA AGGCGTGAGC CATTGCACCC GGCCTTGTGT 240 GTTACTCTTT TTTTTTTTTA TTATACTTTA AGTTTTAGGG TACATGTGCA CATTGTGCAG 300 GTTAGTTACA TATGTATACA TGTGCCATGC TGGTGCGCTG CACCCACTAA CTCGTCATCT 360 AGCATTAGGT ATATCTCCCG ATGCTATCCC TCCCCCCTCC CCCCATTGTG TGTTACTCTT 420 AACTCCTCAC CACAAAACCA GAACGGCCCT GAGACCAAGA CTCAGGTCTC CAGAACAAAG 480 CCCTTAGCCT GACATTCAGG GCCCTTGGCC ACTGGGTCTC AGGAACTGCC GCAGTCCCTT 540 GCAGCCTGTG TCCAGCCTCT CAGAGCCACC TGCCTGCTCC ATTCCTTGCT TCCCCAGACT 600 GTTCCTTCTG CCTGAATGGC CCTCCTGGAC CTCCAATGCC AGGGGCACTC CTATCCAACC 660 TCGAAGAGAT TGCTCTGTCA GTGCAGCCTT GCAGGGCCTC GCTGGGGGAG AATCAGAATT 720 CCTTTCTCCT GCCCTCCCTT GGGCTTCCGG AGCCTTCCGT CATCCTCTAT TTATAGTTCA 780 AGTCAGGTGC CCCTGGACAT GTTGCTGGGA GGGAAGGGCC TCAGCTGGGA GAGCCGGTTC 840 TGTGACCTGC TGGGGAAGGG CTGGGATTTT CCAGGATGCC TCCTCTAGCC CTATAGTCCC 900 CTTGGCTACC TCTGTCTACG GGGAAATGGA GCCCCCTACC TGGACAGCCT TAATCCGGTG 960 CACCTGGTGG CTGCTTGTCT CCTTGGCTTT GCTGTGAGCC CTGGGGCCTG GGGATGGGCT 1020 TCTCTCCAGC CCTGGGCCTG CTCCTGCCTC TGCTGTGGTG AGGTGACCTG AGTAACGGGT 1080 TGGGTTAGGT GGTCTCTATG TTGGTAGGGG TCTCAGTAGG GTCAGGCTTG CTCTAGGAGA 1140 GAGTCACAGT TGCTAGAGTT GAGTATAGAG GGCAGGAACC AGCTGTAACT TTGCAAAGCT 1200 CTGTCCTGGG ATGCTCGGCT TCCCTCCTGT TGTCCTCCAC CTTCCAGAAA GCCCAGCAGG 1260 GAGAGATGAG CACTGTGTCC CCAAACTCAA TGTCACTGTC ACCTCCCCTC ACCCAGCCCA 1320 GCCACTCCCC GTCAGCTCCA GACCAACTCG GAATACTCGG GAAGGTTGAT CCTTCGACTT 1380 CCTCAAGCCA TTGCTCAACA TCCCCCAATC ACAGCCTCCC CAACTCCCAT CTCCAAAGGC 1440 CTCCTTCCTC CCCAGATCCC CGGCTGTCAC CATCCTCATT CTTCTAACAA GCTGACAAAC 1500 TTGAATTCTG AGCGAGCATG ACCTGGGGTC TTGGGCCTGA GCCGCAGCCC TCTGCCTCCA 1560 CCCCATCCCC CACTTACATG CCCACTTTCA GATACAGACA CGGACCCTGA TGCCAAGGAC 1620 ATCCACTGGC TGAATGCCTC CTCCTGCCCT TTCACGAGCT CCCATGCCTG GCCCTGACTA 1680 CCTGCACGCA GCCCTGGACC CTCAAGTGAC TGTAGGAACC CCCTCTACGA GACTCAGCCC 1740 TTTTGCCACC AGTGGGACTT GCAGGCCCAG CTGACCAGCA CCTTCTTGCC TGCTGTGGGC 1800 CATGTGACCG ACGGAATCCC ACCACATCTG CCGTGAGCCT CGCCTGAATC AGGACCAAGT 1860 TTAGGTTTTC AGAATCAGAC GGACGTGACT ATGTGACCTG GGGCAAGTGA CTAACCCTCT 1920 CTGAGCCTCT GACATTTATA GCTGACTCCA ATCTGATACA TGGGCTCCCC AGGGGCCTGA 1980 GGAGGGAAGG TTTGAAACCT CACTCTTCCC TCCCTTGCCC TTGGAAGGTG AGAGCAGGAG 2040 GCTCCTTCAT GGAGGTGGCT AGGATGGGGA GGGAGGACCA GGAAGCTTCC TGACCTTGCC 2100 CCAGGAGCTG GCAGCCCCCA GTCCCACCTT GTCCAGAGAT CACTCAGGGG AAACCACTCT 2160 GGCTGAGGGA TTCAGGTGCT GGTGCCAACT AGGAGAAGCA GTCTAGGGCG CCTCCCAGTG 2220 GACACCAAGG GAACGTCTAT TCTGGCTGGC CCTTGGTCCA GCCCTGTGAT TTTAGCCCTT 2280 GGCATGCAGT CAGGCTCCAG TACTGACCCC AGCACCAGCA GTGGCAAATT GCACCTCATT 2340 TGAGGAATCT CAGTTTCCTC TTCCACAAAA CGGAAATAAT GATAACATCA CCACACAAGA 2400 CCACAGTGAG GCTTCCTTCG GACGACCTAG GCGACCCGCC TTCCACACTA ATGTTTTCCA 2460 GGTCTAGAGA GGCCAGGGCT TGCCTGGGGA CCACAGTGAG ATGTGGTGAG GAGCCAGGGG 2520 TTCAGGCTCT CAGGCTCCTG GTCCACTGCT CTTTCCACTG CTGGGAGGTG CCTCAATGTA 2580 ACCTTGGACT CTCCAGGCCT ATTAACTCCT CCGTGTAGCT CTGGAAGTTT TCAGATGTTT 2640 TAGTGCTATT AACATGCCTG TCCCAGGAAC AAGCTTACAA ATGCATCCAA TTAACCTTCT 2700 GCCAACAATT CTGGGACGTG ATTTCTTTTC 2730
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