Tag | Content |
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EnhancerAtlas ID | HS040-03343 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:223673290-223674510 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat6 | MA0520.1 | chr1:223674140-223674155 | GGTTTCCAGAGAAAC | + | 6.15 | ZNF263 | MA0528.1 | chr1:223674484-223674505 | TCCTCCTCCTCTCCCTCCTCC | - | 11.18 | ZNF263 | MA0528.1 | chr1:223674475-223674496 | GACTCTCCCTCCTCCTCCTCT | - | 6.16 | ZNF263 | MA0528.1 | chr1:223674481-223674502 | CCCTCCTCCTCCTCTCCCTCC | - | 6.27 | ZNF263 | MA0528.1 | chr1:223674478-223674499 | TCTCCCTCCTCCTCCTCTCCC | - | 7.21 |
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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 |
GH01I223499 | chr1 | 223673147 | 223674962 |
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Enhancer Sequence | GGCTCAAGGA GCCCTCAAGA GTAGCATCTG AAGCAGCCAC TGGGACCAGG CTTGCCACCC 60 TTTCAGAGGG GTGTGAGGTG CAGGGCAAAG GGTCTGTAAA GGCTGGCAGG GAAGTGGGAA 120 GCAGTGGAGA GCCAGGACCA GCCCTGGGCA CCCAGAGGGG TTAGGGACCC TGCCACCCCT 180 CCCAGGTTTC CAAACAAGGC CTGTGCCTGC CTGGGCTCTG ACAGTCAGCC AACAAACAGG 240 CATTTCCAGG TCTGCACCAG GCCCCGGGGA TACAAAGAGG AGTGAGAGTT CCTGCCCTCC 300 CTGGATCCTG CGGGGAAGGC TGACAGATAC ACCAATCCTG TGTCACGGGA ACTGGGGATT 360 GGGGGGAATG ATGGGCAGGG GGCATCAGGG TTATCTGAGA AAGCTTCCCA GAGGAGGCGG 420 TCCCTGGCTG AATTGAAGAA ATTGCTGGGA GCTTCTCAAC AAGAGCATTA GAAGGGAGTT 480 GGGGGCACGA AGTGGGTGCT CATGTCAGGA GAAAAATCCA CAAAGGCCTC TCATATGCAC 540 TCTGCGCCCT CCTCTCATTT TTCCAGGGTC CTGCTCCCAG CTGTGCAAGC TGCAAGGAAG 600 AACGAGCCCC CTCCTCCAAG GCCTCGACGG TCCACTCAGT CACCCACTTA AGAATTCACC 660 AAATAAGTAA TGACTAAGTC TGACTGGGAG AAAATGAAAG CTCTCTTGGA GGGGAAAACA 720 AGTTACTCAT GCAACCAAGA GCATATCCTT GGCACCCTCC ATGAGTGGAG CCACGGCAGG 780 AGGGGCAGAC AGGAACAAAC GGTGGCCATG AATCATGCTG TGTGCGAGCT CCTTTGTTTC 840 TAAGGCATGT GGTTTCCAGA GAAACCAGGG AACACTGCCT TCAGGTAAAC ACGCCCACCA 900 CCCATGCTTC TTGGAACAGG CTCTGTCCTC CAGGAGCCCC ATTAAAGAGG CCTAGCTGCT 960 TACATTTGTC AGTTGTACTT CCACAGGGGG GATTTCAAGT GCTAGCTGGC CAAGTCATCC 1020 AACGGGTGGC AATGGACCTT CTGTTGGCCG GGAGCATCCT ACCCCGTGCC AGGTCCCTGG 1080 TCCCACTCTG CCCACCACCC TCTCACCCCC AGAAGAAGAC TCCTCTGGTT GATGAGTTTG 1140 GCAGAAGAGT CTTGGTTTGG TCAGTTCAGC CCTTCTGCTC ATGCTGACTC TCCCTCCTCC 1200 TCCTCTCCCT CCTCCGCTTC 1220
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