Tag | Content |
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EnhancerAtlas ID | HS120-02938 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr17:78004350-78005090 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr17:78004577-78004588 | GCAGGGTGTGG | - | 6.62 | NHLH1 | MA0048.2 | chr17:78005049-78005059 | CGCAGCTGCG | + | 6.02 | NHLH1 | MA0048.2 | chr17:78005049-78005059 | CGCAGCTGCG | - | 6.02 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27830 | chr17:78003903-78005259 | Fetal_Intestine | SE_28735 | chr17:78003096-78005528 | Fetal_Intestine_Large | SE_30858 | chr17:78002351-78005662 | Fetal_Muscle | SE_41917 | chr17:78002621-78006297 | LNCaP |
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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 |
GH17I080028 | chr17 | 78001967 | 78005454 |
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Enhancer Sequence | TCCTGGAGGT AGCCTGGAGC CACTAGGAGA GAGGTATCAC CCCAGCCTCT TCTCTTGCTC 60 ACTCTGTGCC GTGCACCGGC CTCAGGGCCA CCTTGGGTTA GGGGCCAGGA TGCAGCAGTC 120 AGCAGGACAG ACCTGGTCCT GGAAACCCAT GGAGCTGGCA GTTCCCACTC ACCAGAGGGA 180 CGCAGCCCAT GCCCACTAGT GACAGGCAGG GGCAGAGGCA GAGGCAGGCA GGGTGTGGGG 240 GCCACGGGAC GCAGCCCACC ACCGATTATT CCCATGGCCA TGTCACTGCC AGACTGCTCA 300 GGAGCAACAC GCACTGAGCC CGGTCACCTG GCACATGGCC GGCAGAAACT GGTTCATCTG 360 CTTTGCCCTC AAAGCCCAAG CAACAAAGAA CAGGGAAACA GCGACACCTT ATTAAACACG 420 AGCCAGACAC ACGCAAACAA GGATCGCGTT GCCCCCGCTG CAGAACGTCT GCTGCTGGCA 480 TGCCTTGGAT GAGGCCCCAG CTTCCTCCAC CTGCCCAGAG CCAGGCAGGG GCCCTACCCA 540 TCTTCCTGGG AACCCCTGGC TTTGCGGGTC AAAGGGCGAT ATGGAATCTT GTAGGCAGCC 600 AGGATCAGGA CCCAGTCCCC GGGCAGCAGG CTTGGGGAAG GTAGCTCCTT CAGTCTCATC 660 AGGAGGATAA TCCCCTGCGG GGCCGCCGTG ATTTCTCCTC GCAGCTGCGC TGAACTTCAA 720 GTTACAGGAT GAATTGAGAA 740
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