Tag | Content |
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EnhancerAtlas ID | HS040-01131 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:27706690-27708260 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:27707652-27707673 | GGATGAGGAGCAGAAGAGGGG | + | 6.27 | ZNF263 | MA0528.1 | chr1:27707649-27707670 | GGGGGATGAGGAGCAGAAGAG | + | 6.29 | ZNF263 | MA0528.1 | chr1:27707194-27707215 | GGAGCAGGGGGAGAAGTGGAG | + | 6.3 | ZNF263 | MA0528.1 | chr1:27707655-27707676 | TGAGGAGCAGAAGAGGGGAGA | + | 6.3 | ZNF263 | MA0528.1 | chr1:27707191-27707212 | GAAGGAGCAGGGGGAGAAGTG | + | 6.49 |
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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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Enhancer Sequence | GGGGTGAGGC AGGGCAGGGG TCATAGCAGT CACTGTGAAC CAGGATCCCA GTCCTACCCT 60 CATAACTGGC ACAAGTAACC TGGAGGCCCC GGTCCTCAAT ATGGGGTGCT TAAACCCTGG 120 GCTCCGTTTA GTCCAGATCC CGCAGGCAGT TGGGAAGCGC CTGGTGGGAG GAACAGTGGC 180 AGGGGAGGGT GGGGTGCTGT CCAGCCCTGG CTCTGCTCCT GGCTTGCTCT GTGGCTTTTA 240 TGCCACCCAC ATTCTCTCTG GGCCTCATGA TCACATGGTC CAATTGGTGG CTTGGACCAG 300 TGACTGGGCT CCCACCCTCC CTGGGCCTCA CCAGCCCAAT AGGGTGAAGA CAGAGCCAGA 360 ACTCAGACCC TCCCCTGCTC ACAATTCCTT TCAGCCTTGG ACCTCAGGGT TCAGAGCCAA 420 GATGCAGACG ATATAGTCCC TTTTCAGGAC TCCTAAGCCC TAAGACCTCA GTGTCACCCA 480 ATGTCAGAGC CCTCAGAGAG GGAAGGAGCA GGGGGAGAAG TGGAGGCCCC AACTGTCACC 540 CTGCTAAGTG GGTAAGCGAG GACTGGACAG TGTGTGTCAG GGGGAACATG GCTGAGGGAC 600 AGGCTTGGCC AAAGTCACCT CACAGGACAT AGCCAGACTC ACACAGGGTC CCCTGACCAT 660 CTCCTCTGCC CCTTAGAAGG TAGGGCTTTA GGGCCATGGT TGCCAGGCTA TGCCTGGGTG 720 GCTCCCAGCT GTGCCACGGT ACCTGTCCAC TCCTAGCAGG GATTTGATTT CAGGCCCTGG 780 GCTGGGTGCC CAGAACAGGG CAGGGCTGGT GGATGGAAGA TCATTCTGGG ACAGTGGAAA 840 GGGGCCCAGC CTGAACTGGG TCTCCCTCCC AGAAGGTGTA AGGGGTGGAA GGAGTCTGAC 900 AATATGAAGG GCAAACAGTG GTCCCAGCTC CCGCTCAGGG AGCCCCAGAG AAGGAAGCTG 960 GGGGATGAGG AGCAGAAGAG GGGAGAAATG AGCCACATGA GGCTGATCCG GGGCTCCAGC 1020 TGAGGGAGCT GAGCCATCAA TAATTCAGCT TCTGAGATCG GTTTCTGGCT TTAATTAACC 1080 AAGGGCCTCT TCAGCCATCC CTGCCAAGTC TGGTGACCTC CAGCCCCTGA GAGGGAGTGG 1140 GAAGCAAAGG GTGGCATTCT TGCCTCTACT CCGCCAGGAA CCCGCCTTGT GACCCTCTCT 1200 GGGCCTGGAG GGTGCAGTAG GCAGGCACTG AGGATGTCTC CTGAGCAACT CGAGCCACAC 1260 ACCCTCACCT CCAAGGACAA GTCCCGAGGA GTGACCTTGA GTTCCCAGAA CTGGCAATGG 1320 GGAGGAGGGA TGGGAACTGT CATTTCTTGA TTGCCTTCAG TGAGTCAGAC ACTGAAGTGG 1380 GCACTGTACA GCTTCTCATA AAACCTGCAG AGCAACTCTA TGAGAAAGGC ATCATCCAAC 1440 CCATTTCACA GATGCGGAGA CAGGCTCCGA GGGAGAAGGC GCAGGGCCGA GGTCACAGAG 1500 CATGTCAGTG CCTGAGCCCA GAGCTGTCTT CCCCTGCACC TCTGCTCCTC CCACTGCCCC 1560 GTCTCCAGGG 1570
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