Tag | Content |
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EnhancerAtlas ID | HS007-02593 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr10:134385400-134386370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr10:134385630-134385641 | GGTGACTCATC | + | 6.32 | JUN(var.2) | MA0489.1 | chr10:134385626-134385640 | AAAAGGTGACTCAT | + | 6.89 | JUND | MA0491.1 | chr10:134385630-134385641 | GGTGACTCATC | + | 6.62 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_02231 | chr10:134384577-134386446 | Aorta | SE_04270 | chr10:134384937-134386427 | Brain_Anterior_Caudate | SE_10679 | chr10:134383802-134386494 | CD19_Primary | SE_11174 | chr10:134383318-134386815 | CD20 | SE_41657 | chr10:134383727-134386549 | LNCaP | SE_54289 | chr10:134384177-134386431 | Spleen | SE_61574 | chr10:134349316-134386582 | Toledo | SE_62964 | chr10:134349568-134409019 | Tonsil |
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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 |
GH10I132570 | chr10 | 134383893 | 134386565 |
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Enhancer Sequence | TGTTAACGAC CGACTGGGCT AGAGGCAGAG TGGGCCGCAC CCTGACCACC ACCTCTGTCC 60 CCCACTGCTG TGCCCCTCTG TCTCACTGTT TCCTGTGGTC CCTCCTGACT AGAAGAGACT 120 CAGGCCTGCT GAGTAGCATG CAGCACAGGA CGAGCCTGCA GAGCCCTCTT GGGACTTACA 180 CACTGGGGAT TTGACAGCTC ATGTCTGGCA CCGCAGATAG TCTAGGAAAA GGTGACTCAT 240 CCAAGAGCCT GGCCGGAAAC CCACAGGGTA TTGGCCCAGG TGTGCCGAGA GGCTGGCCGG 300 AGGGACCATT GTGATACTCA GAGGAAAACG CCTGTGGCCC ATGGGGGGGC CTTCAGAAGA 360 ATGTCGGAGT TTCTCAGCTG GCAAGATGCC CCTGGTGGCA AGATGCCCCT GGTGGCAAGA 420 TGCCCCTGGT GTGGGGCCCC TCACCTGGAC CAGAGGCCTT CCCTGAGCTT CTGTTTTGCA 480 GGGAGGTGCC TGAGCTGCAC AGCTTGCCTG GGAGGAGTCG TGGTTTCTGG GGGTGGGGCC 540 TTTCGTAGGG CTGTGCTGGT GCTGTCCTGG GGGAGGGGGA TGCTGAGCAC GCCCGCCCGG 600 GGCTGCTTTC CCTGGGAGGG ATGCTGAGGC TGCCCAGGGC TGCTTTCCCT GTGAAGCAGC 660 GTGACCCAGG GCTCTTGGTG GGGATGTGCC GTTTGCTCTT TTTCATGTGT CTAGCCCTTG 720 GGAAGTGTTT TTGGTACTGC TGGTTCTCAT GCTCTAGTCC TGGTAATGGG CTAGTGTGCT 780 TGTTCTGGCT TTACTCGGTA GCGTTTATAA CAGGACAGGA TTCAGAGGAC ACTGTTGCTG 840 AGGGAAAGTT TGTGCCACTT AACCTGGTGT TGCTTCTGGC CCTGCCTCTG CTGGGCGTCT 900 GTCTGCAGCG TGCCTTGGAG TGTTTCCCTT GCTCTGCTGA TTGCTGAAAT GCAAGACCTG 960 GGCCTCTGGA 970
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