Tag | Content |
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EnhancerAtlas ID | HS034-09333 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr14:90167470-90168510 |
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 | GTTTAAATGG CCCTCGGGAA ATAACACTGA TTTTCAAAGT CGTTTTAAAA GGCAGCTTTT 60 GGCAGCTGCT ATCTTTTGCA TATTCTCTTT CCGAGATTAA AGAACCTTCA GGTGACAACA 120 CCTAGGGTAA AAGGATGGGA CATCAGGCTG CAGACGTGCG TATGCGTGTG TGCACACGCG 180 TGCAGTCTTG ACTAGGTGTG GAAAAAAGGT CCGAAGAGAT TCCAAAATCA AAAAAATTCC 240 CTTGGCCTAC TCCGGCCCCG AAGACCAACT CAGACCCCAC CAGACAAACT GGAAAGTCTC 300 CAAGCTCTCA GTCGCCCCAG TCGGCGGGGG AGTGAGTGGG GCCGACCGGC CTTGCGGCCC 360 TGCCACCTTT CGGGGCGACT CGGTTTCTCC ACTGACACCC CCGGGCGCGA GGTCTGGTCC 420 ATCCCGGAGT GGGAGCTAGG CAGGGACGCC ACCTGGCAGC CCACTCTGGG CCCCTGGCCC 480 GCGTTTCCCG CAGGCGCCGG CGGCGTCGGG CGCGGCCGCC GCGCTGCCAT GGCAACGGCG 540 GTCCGCCCCC CCCCCGCTTC CCGGCGCCGG CGCGCCAGCG GGGCGGGGCG GGGCGGGCGT 600 TGCTAGGAAA CCGGCGGCGG GCCGCCTCCG CGGCGCGGTC TCTCGGCTTC CACCCTTCAC 660 CTACTTCCCC TGCGGGGCCG GAGTGGGGGA GGGTCGGGGG AGGCCATCGG GAAGCCACGT 720 GGTGGCCCGG GGCCTCGCGG CTCATTCTGC GTTGCGCCGT CCCTTCCAGG TCGAGTTGAC 780 GGCCTTTTCC CCCTTGGCGT ACAAGTATTG AGTCCCGCGC CCTGGGAGGG AGACGGCGCT 840 CAGCAAATTT AGATGAATGC AACGCTTCAA CGTGGGCTCT CGACCTCTGG TCCCCCATCC 900 CCTGCCGGCT CTATTAGGAC AATGAAGTCC CCAAACTCCA CTGGAGGGTT CTTCACCCAC 960 TCTTCTTCCC CTCCAAAGGA ACCATCTCTT GAACTTCACG AAATCCAGGA GCAATGCTAA 1020 GCGTTTTGTA TACATCACCT 1040
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