Tag | Content |
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EnhancerAtlas ID | HS182-03355 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:1908810-1911310 |
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) |
Mafb | MA0117.2 | chr11:1909889-1909901 | AAACTGCTGACT | + | 6.22 | NFIA | MA0670.1 | chr11:1909804-1909814 | GGTGCCAAGT | + | 6.02 | Zfx | MA0146.2 | chr11:1910013-1910027 | GAGGCCCAGGCCCC | - | 6.08 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_00878 | chr11:1910432-1913105 | Adrenal_Gland | SE_02963 | chr11:1909275-1910120 | Bladder |
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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 |
GH11I001887 | chr11 | 1908980 | 1913595 |
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Enhancer Sequence | GTCCCTGGCA ACTCACAGAA GGGGATGAGG TGCACACACG TGCACTGTGC TGGGAACTTG 60 GCAACCTGGA GGCTGCCTGG AGCCCTGTTG CAGGCTACAA GGGTGGACTC CGAGTTGGCC 120 AGAACCCAGA CCAGCTCAGT CTCCCAGTCC TGTGCAGATG CTGCCTCTCT CACCTGATAC 180 CAGATTCAAA CTCTCTGCTC ATTTCACTAG AGTCAGCCCG GCTCAGCCAC TGCTCCACTA 240 GGGAAGCTCA AGGCTCCCAT CTGGGACTCC CCAAAAGCCA CAGCAGGGCT CGTGAGGGAA 300 GTGAGGGGCA GCCTGGCCAC CACAGGGCTA GCATTGAAGG AAGCAGGTGG CATGGAGCCC 360 AGGTTCCCTG ACCATCTGTA TGCTGAGGGT CCATAGAGGG GCAGGAACTT AGGTCCTACT 420 CCCTGTCCCA GCCGAGAGCG ATTCAGAGGT CCTGATGCCC TCCCCATCCC ATGCTGCAGA 480 CAGAGCAGTG CCACTCCTGC CATGGTGAGA CACACATTTA TTAGTGACCT GGGCCCCAGG 540 CTCCATTTCC AGCACCCATC ACACCACAGG GTGGGGCAGC TGTCCTCCTA CCATCTTCCC 600 CTGCCAAACC CTGACTCTCA AGCAGCTGTG GCAGAGGCTT TTTCTGGTAC CTCTGTGTCC 660 CTCTCCTGTG GTTGGCCACC CCCACCAGAG CCTGGCTGAC TGCTGAGTAG GCCCCTCCAC 720 TCTCCCCACC AGGGCCACAG CCCCTTCTCT GTCCCGCTTG GCCAAGCTGT TCCCATAGGG 780 TTGGGACTGA GGGCTCCCTC CTCATCCAGC TGTCAAAGCC TGGGCATGGC CAGTGCTGAG 840 ACCCTCGCTG TCCCACCAGC GAATCCCTCG AGTTCTGCCC CCTCAGGCTG TCAGCCCAGG 900 TAGGGGAAGC AGAGGTGGGC CGAGAGAGAG GTCACGCTGG GCCCTCCTCC ACCCCTGATG 960 AGCCCCTCCC TGCCTGCCCC TGAGCACTTG TATTGGTGCC AAGTCCCACG CTGGCTGAGG 1020 GCTCCCCCCT GCACCCTAGT CCCAGGATCT GGCTCTGCCA TCAGGAAGCA CAGGCAGCAA 1080 AACTGCTGAC TGCTCCTGAC GCCGATGGCC AAGCCAGCCT GACCGCACCC ATGCCTCAGC 1140 AAGCAGAGAT CTGGCCCCAA ACCTTTGACA GCAAAAGGTG ACAGCAAAAG GGAGGATCAG 1200 TGAGAGGCCC AGGCCCCTGA GGAGCCTGGG CTAGGTCAGT AGATGCAGTC CTCTGCCATC 1260 TTACCTAAAG TTTTCATCCC AAGGCCCCCA TCCTACATCC CGACGCAGAC CCCTTCTCTG 1320 TTCCCCTCAC ACCACTGCAG CCCAGGGGCT CCAGCTCGTC CTCTCTGCCC CGTCCACCTG 1380 ACCACCCTCC TAACCATGCA GACTTCCCTC AGCACCCCAT GTGCCCTTCC CAGGCTGCCC 1440 TGCACCCCAT GCCCCTTGGG CCCTGGTGCA TCTTCATGCA GCAACTATGG GCCCCCAGCT 1500 AGAGCCTCAG CCCCTTCTTC TGTCCATCCC ATGGTCCTGG GCTCTGGGGG CCATTCTGGC 1560 CACTTCACTG GAGCCTCCAG CCAGTCGCTG TGCGGTTGAA GTTCTTGGGC TGGGGGCTCA 1620 GCTCCAGGAT GGAGCGGACT GTGGGAGGGG GCCGGGTGGC CTCCTGCAGC TTCCGGGCGT 1680 TGAAGCGAGG CCGGTACAGG AAGGGCAGGC GGGTGAGGCT GGCTGGGGTG TGCTCCCCAC 1740 CGCTGGGCCC TGCCAGGCGC CCTTGGGCCT CCGCCACTGA CATGCGGTAC AGCACGGCAT 1800 CCCACATCCT GGAGGTCCGG GAGGCGGGGG CCCGGGGTGC GGTGAGGGCG GGCACCTCCT 1860 GCTCTGTGGG GGCAGGCACC TCCTGCTCTG TGGGGGTGGG CACCTCTGGC TCCAGGCTCT 1920 GCCGCGGCTC TGGGCACGGA GGCTCTGGGG CCTCCTCCAG CAGCTGCTTC TTGAGCCACG 1980 TCCAGCCACT GAGCCGGGGC TTGGGTGCAA CTTTGGGGAC AGGGCATGGG TGAGGGCCTG 2040 ATGGTGGGGT AGGGGATGAG GCCCAGGCAG GGCTGGACAC TCGCTCGGCC TCAGCGGCGG 2100 GGCCAGCCAT CGGGGGCTCC TCCAGGTGCT CTCTGCCAGG GCCCATGGGG ACCAGGCTGT 2160 GCGGTGAGGA CTCCAGCGAG CGGCAGGTCG GGGCTATGGG CACCACAACC CTGGCACTAG 2220 CCTCTCTGGG CACTGAGGCC TGGAAGCCGG GTGGCGGCCG TGGTACAGGG GGCTCCTCAG 2280 GCAAGGGACT GGCAGCCTGG ACTGTGGTGG GCAGTGGGCG GATGTGAGCC ACTGGGACCA 2340 GGGGCTGGGC CCTGGGGGGA CTTGGGGTGG CATCTCCATC CTGGCTGTTG GATCCCACTT 2400 CTGGGGCTGT CCTGGGAGGC TCAGGGGTCC CATTGTGTGG GGATGGTGCC AGCTGGATGT 2460 GCACCTGGGT GACGTGGGTG CCCCCACCCC CAGAGACAGG 2500
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