Tag | Content |
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EnhancerAtlas ID | HS052-07477 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr11:103196510-103197730 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr11:103196723-103196743 | CAGTTGGGTTTGGTTTGGGG | - | 6.27 |
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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 |
GH11I103325 | chr11 | 103196341 | 103197485 |
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Enhancer Sequence | TTTTGTTGAG CTTTTTTGCC ACATTCTGCA TTCTACGTCA TTTCAGACAT TTCAGTCTCA 60 TTAGGGACCG TTGCTGGTGG GCGGGGGATG GGCGTATAGT GGGCTCCTTT GAAGGTAAGG 120 GGACACTGGC TTTTTGAATT GCCAGAGTTT TTTCTCTGAT TCTCATCTGG TGGGGCTGGC 180 GTTCCTTTAA CTCTGATGCA AGTTGGGTGC ACTCAGTTGG GTTTGGTTTG GGGCGCTTTC 240 AGAGGGCCAA GGCTCTGTAC AGTGTCTTTA TTTGTGGGTG AATTCTTGCT CTTGGTTTCC 300 GGCATCTATT AGCAGAATAA TGTTTAGTGT TGTAGTTTGG GCTTCAGTCC AATAGATGGC 360 GCTTAGGAGT AGTGGCTGGT AGATAGGCTC TTACTTAGCC CTGTGGTTTT TTTGTTATTT 420 CCTTGTTTTC GCAGGCACGT TCTTGGGAGT AGAGGGAGGG GCGGGGAATA AAATCATCTC 480 ACCAGGGCCC CGTCCTTGGC TTTGAGTGAG CCTCTTCTGA TCATTGGCTC CTTCCCCGGG 540 TTTCTTTTGC TATGTGTTCG GGGTGGTTGG GCTCCCTCTG ACAGGCTGCA TCCGGGAGAT 600 AGGCCGGCCA TACGCTTTCT GGGCCAGCCC TGTGGAGGGA CGTACGAACC GCCTCTGTGC 660 TGGCCCACAA ACCTGCACGT CCCACCCCTC TCAGTGATCT GAGGGTGGGC GCTTCTCCCC 720 AGCTCCAGTG TTGGCCGCAG ATCTGGGCTC GGTACTCCTG AGCTGCAGAC CGCATTCCGG 780 GGACACTGGA ACAGCCCTTG GCTTGGGGTC AGACTCTGGC AGCACTGGGG GATCTGAAGT 840 GCCCCTAGGT TACTTGGAAA ATACTCAGAT AGTGCGGAGC ACTCAGGCAG GGCTGTGGAG 900 GCTGCGTTGT GCACACGATC CTGCGGGGTG GCTATGGAGG GGCTCGGCAG TGGGAAGGCC 960 TGCAGAACAG ATGTGCCCCA ATCCTGTGGG GGAAGCCAGC CTGCTGTCTC TTGGCCTGGC 1020 AGTCAGCTGA TGCTAGAGCC TCTAGGAGGG TGATGAGGAC CCCTGGGGGA ATGGGCACTT 1080 AGGGCCTTAC TCTACTACAG CTGTCCTGCA CACAAAAGCT CCTGAGCTCC ACAGCAGCTG 1140 AAGCACTGTT TCTGCCTAGT CTCCAGGCAG ATCCTCCACC AGCTCACACA TCCATGGTGG 1200 ATGCGGGGTC CGCTGAGCTA 1220
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