Tag | Content |
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EnhancerAtlas ID | HS059-14568 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr14:90167650-90168690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr14:90168049-90168059 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr14:90168054-90168064 | GGGGCGGGGC | - | 6.02 | RFX1 | MA0509.2 | chr14:90167991-90168007 | CGCTGCCATGGCAACG | - | 6.21 | RFX1 | MA0509.2 | chr14:90167991-90168007 | CGCTGCCATGGCAACG | + | 6.22 | RFX2 | MA0600.2 | chr14:90167991-90168007 | CGCTGCCATGGCAACG | - | 6.44 | RFX2 | MA0600.2 | chr14:90167991-90168007 | CGCTGCCATGGCAACG | + | 6.4 | RFX5 | MA0510.2 | chr14:90167991-90168007 | CGCTGCCATGGCAACG | - | 6.82 | RFX5 | MA0510.2 | chr14:90167991-90168007 | CGCTGCCATGGCAACG | + | 6.92 | ZNF740 | MA0753.2 | chr14:90168012-90168025 | CCGCCCCCCCCCC | + | 6.64 |
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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 |
GH14I089700 | chr14 | 90167226 | 90169650 |
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Enhancer Sequence | TGCAGTCTTG ACTAGGTGTG GAAAAAAGGT CCGAAGAGAT TCCAAAATCA AAAAAATTCC 60 CTTGGCCTAC TCCGGCCCCG AAGACCAACT CAGACCCCAC CAGACAAACT GGAAAGTCTC 120 CAAGCTCTCA GTCGCCCCAG TCGGCGGGGG AGTGAGTGGG GCCGACCGGC CTTGCGGCCC 180 TGCCACCTTT CGGGGCGACT CGGTTTCTCC ACTGACACCC CCGGGCGCGA GGTCTGGTCC 240 ATCCCGGAGT GGGAGCTAGG CAGGGACGCC ACCTGGCAGC CCACTCTGGG CCCCTGGCCC 300 GCGTTTCCCG CAGGCGCCGG CGGCGTCGGG CGCGGCCGCC GCGCTGCCAT GGCAACGGCG 360 GTCCGCCCCC CCCCCGCTTC CCGGCGCCGG CGCGCCAGCG GGGCGGGGCG GGGCGGGCGT 420 TGCTAGGAAA CCGGCGGCGG GCCGCCTCCG CGGCGCGGTC TCTCGGCTTC CACCCTTCAC 480 CTACTTCCCC TGCGGGGCCG GAGTGGGGGA GGGTCGGGGG AGGCCATCGG GAAGCCACGT 540 GGTGGCCCGG GGCCTCGCGG CTCATTCTGC GTTGCGCCGT CCCTTCCAGG TCGAGTTGAC 600 GGCCTTTTCC CCCTTGGCGT ACAAGTATTG AGTCCCGCGC CCTGGGAGGG AGACGGCGCT 660 CAGCAAATTT AGATGAATGC AACGCTTCAA CGTGGGCTCT CGACCTCTGG TCCCCCATCC 720 CCTGCCGGCT CTATTAGGAC AATGAAGTCC CCAAACTCCA CTGGAGGGTT CTTCACCCAC 780 TCTTCTTCCC CTCCAAAGGA ACCATCTCTT GAACTTCACG AAATCCAGGA GCAATGCTAA 840 GCGTTTTGTA TACATCACCT CATTTTCAAT CCTGTGAGGT GGGAGCTGGG AACTTCATTT 900 TAACAGGAAT AAAATGTGGC CTACAGCTGG TTGGGGTGGA GCCAGGACTT GAAGTCCAGT 960 TGTGCTTATT AACTTCAAGT GTCTGCCTTT TTATAATGCT CAAGTTCGTC CTCTCAGCTG 1020 CCTCTTGGCT AGCCCAGCAT 1040
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