Tag | Content |
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EnhancerAtlas ID | HS092-29055 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr3:134144820-134146660 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr3:134145044-134145056 | AAACAAACAAAC | - | 6.32 | HES2 | MA0616.2 | chr3:134144911-134144921 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr3:134144911-134144921 | GGCACGTGCC | - | 6.02 | STAT3 | MA0144.2 | chr3:134145637-134145648 | CTTCTGGGAAA | + | 6.62 |
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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 |
GH03I134426 | chr3 | 134144883 | 134147981 |
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Enhancer Sequence | ATCTTTGAGC CCAGGAGTTT GAGACCAGCC TGGGCTACAT AGTGAGGCCC CATCTCTACA 60 AAAAATAATA AAAAATTTAG CCAGGCATGG TGGCACGTGC CTGTAGTCCC CGTTGCTCAG 120 GAGGAGGTGG GAGGATCGTT TGAGCCTGGG AGGTCAAGGC TACAGTGAGC CATGATAGTG 180 CCACTGCACT CCAGCCTGGG TGACAGAGTG AACCACTGTC CCAAAAACAA ACAAACAATA 240 GTTCAAGTTA AGGAATGTCC TTGATTAGCT CCTGCTTGGG GTTTCAGAGG AATAGCTTAC 300 TTTGTCTGAG AAGAGCCTAA AGCAGCCTTC CTTCTATGGC AAAGCCTCCC TTTTACCTTT 360 TTCTTCTTTT GGGGGCCCCC TCTAAGCTCT CTCTGAGGCA GGCCCTTAAA ACTCATCTCT 420 CAGCAAGGCT GGGTGCTGGC ACTGGAGACT ACATAGAGGT GATAAGACAG AGACTCCTAA 480 CTCAGTAAGC TCACAGGGAG ACCTCCCACC TTGGAAAGAC AAGGCCTTCT TTCAGGTTCA 540 GCTCACACTT TCACTGCCAG TGTGACCTAG GCCTCAGTTT ACCCATTTGT TAAATGAGGA 600 GGCTGGCCTA CATTAGCCTT CCTCCGGGTG TCAGTCATGT ACAGTAGTCC CATATGATGC 660 TCCAGGGACC ATACTTTGGC CAGTAGGTTC GCAAGTCACT GACGCCTGTG GGAGCATCCT 720 GGGAAGCCCA CAGGCTGCAT TGCACCCAGG TCAAAGCTGG GGCTGCTCAC TCTAGCTGGA 780 ACACAGAGCC CTTTACTGCT GAGTGCCTGC AGGCAGCCTT CTGGGAAAAG CCAGCTGTGG 840 ATTTCTAAAG GACTTTCCCA GGCAAAGATG CCTGGGATAA GAGAAAAACA GGATGGTGAA 900 AGCACCATCC CAGGGATGTG AGGGATGGAG CAGCCTCTCT GACCCGAGAC CTGTGGTTGC 960 ATCCCTGCCT ACACTGAGCT GCTCCAGCTG CATCAGGCCT GACTTTGCAG GCTGGTGGTT 1020 AAGTGGGTAG ACGGGTCTGG ACGCACAGCC ACTTCTGGTC ATCCACAGCG ATGAGCAAGC 1080 GGGAGTTTCA CTGCGGCTGC CTCTGACACC GTGCTTCATC CCAACCTTTC TCACAGCCTC 1140 CCTCAGTGTT TCCAAGATTC CCTGGGGTGA GTGAGACTCA TGGTGAAGCT CAGACTCTAC 1200 CATGGAGGGC AGGCCTGCCT CACCTGGGGG CCTCCCTGAA GGGGTCACAA GGAGGTCTGA 1260 GGGCAAATAC ATCTCCTTGG CTGGCTCCTA GAAATGAAAG AGGGGCAGGA TGATCAGAGG 1320 AGTAGAATTT GACTTCCTGG TCCCTCCCTG TCCTCCCTCA AGAAAGAGGT GACAAATGAA 1380 GCATTCTTGG GGAAGGAGAG AAAGTCCACA GTGACTGAGG TCTGAGGGCA GGGCTGAGAC 1440 AGTGGTGGTG GAGATGGCGA CCTCAGCCCT CCACACGTGC AGTGTCAGGG CCTCGGAGCC 1500 CAGCTGGCAG GCCACAGGAG ACAGCGGGAG GTCTGGCTGG AGTGGAGACT GAGTCATCTG 1560 GGACTGCAGG GTCCAACGGA GTCACGCCTG TGAGTGATGA GCACCTTGAC TGAGGCCAAC 1620 GTCACAGACG TGTCTGGGAA GTGAGTCAGG GACCCGCAGA GTAGGAGTCT CAACATTCCT 1680 GGGAACAGCT TCCTCTGACT GTCCTGCCGT GATATGTTTT CTCCCCTAAG TGGCCTCAAA 1740 GGGTTGCTGG CTTTGCCATT GACATTTCTA CAGCAAAATG AGCTAGTGAG CACTGGAGTT 1800 CAAAGGACAT GGTGCAACTT TCAAACCAAA TTCTCGTGGG 1840
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