Tag | Content |
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EnhancerAtlas ID | HS040-03113 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr1:206655480-206656500 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:206655604-206655622 | GGAGGGGAGGAAAGAAGG | + | 6.84 | HOXA13 | MA0650.2 | chr1:206655663-206655674 | CCCAATAAAAC | + | 6.62 | Klf1 | MA0493.1 | chr1:206656017-206656028 | TGGGTGTGGCT | - | 6.14 | ZNF263 | MA0528.1 | chr1:206655601-206655622 | TGAGGAGGGGAGGAAAGAAGG | + | 7.06 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 206655572 | 206655672 | chr1 | 206655916 | 206656391 |
| Enhancer Sequence | GAGACAGAGA AGAAAAGGGC CCTGTTCGGG GGAAAGGAGG GGATGCTGGG GAGGCTTACT 60 GAAGCCACAG TCATGATGGC AGATAGCCCA GAGCTAAGCC AGAGGCGGAC AGAGGTGGAG 120 GTGAGGAGGG GAGGAAAGAA GGCATAGAGG CCCTGAAGGA GTCCAGCTAG AGAGAGGTTG 180 GACCCCAATA AAACAACCAG TAGAGAGCCA TTGTAGATTC TTGACCTGGA AAGATGTGTT 240 TGGGAAAGCT TTTTGGGTGT CTGTCTGCCC ACTTGCCCTG GATGGACAGG CATGGTGGGG 300 AATGGCACGC TGGCCTGGGT CTGGCGTCCT GGCATCCTGG TGTCCGCTGG CTGCTGTTCC 360 CCTGTTCTGG CTCTGCAGCC TCCTCCAAGG TGGCCTCCGT GGTGTGTCTA GAGAGCTGGG 420 GTCAGGCAAG TGCCTGCTTT GAAGCCTATT TCAGCCTCCC ATCAAGGAGG AGGATGGTGA 480 GCAAAAACAG TTGTGAGCAG GGAGCCAGAG GGCCAGGTGC AGCCTCTTCT CTTAGTCTGG 540 GTGTGGCTCC AGCCCATTGT CACCTTCCCC TACCTGGGCC TCTGTGTCCT CATTTTCAAA 600 ATGAGAGGGT TGCATGATCT CTGCGGCCTC CCAGCTCCCA CATGTTGCAA GCCCATTCTT 660 GCCTGAACAT CCCCAGACCT GTAGATTCTC CTAAGGGCTG AAGACACTAG CTCCACCCGC 720 AGTGGAACCA GGTATTTTCA TGAGCTGAAT GTCACACTGG AGGAACCCAG CACCTCATGC 780 CAAGTGGCCC ACCTTTGCCC ATCCTGGTGA CCCACCTCTC CCCCAGTGTG CATATCCTGC 840 CTCAGGTTCC CCAGGACAGG TCCTTTGGTA GAGCAACCTT GCCTTTGTCC CAAAGCTCCC 900 TGGCCCTCCT GGGCAGCTGC TGCCATCCAC AGGCACTGCT CAGGCAGCCA GGACGGGCTT 960 TGGGAATCCT AGGGCTTCCC CCAGCCCCGC CACCAGGCAA GACATTCCAG GCAAGACTTC 1020
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