Tag | Content |
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EnhancerAtlas ID | HS040-03712 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:249166960-249168440 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr1:249167156-249167168 | TCTAAAAATAGA | + | 7.22 | MEF2C | MA0497.1 | chr1:249167154-249167169 | AGTCTAAAAATAGAA | + | 7.58 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_12804 | chr1:249167545-249167799 | CD34_fetal | SE_21287 | chr1:249165758-249169105 | CD8_Memory_7pool | SE_42088 | chr1:249167099-249168183 | LNCaP | SE_43352 | chr1:249166222-249168985 | Lung |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I248871 | chr1 | 249165877 | 249169108 |
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Enhancer Sequence | TTTTAGTAGA GACGGGGTTT CTCCATGTTG GTCAGGCTGG TCTCGAACTC CCGACCTCAG 60 GTGATCCGCC CACCTCCCAA CGTGGTGGCG GGATTACAGG CATGAGCCAC CGCGCCCGGC 120 TGCATGACAT ATATTTTAGT TTTTGAAAAA TATTTTAGCA AAAGTCACTT TAGTGAGGCC 180 TTACTTAACT GCACAGTCTA AAAATAGAAC TTCTCCACCA CTTCATTGCT TTTGGTTTTT 240 CCTCACACTC TGTACATGTG ATTGTGCTGG TCATCTCCTT CACTAGCAAA TCAGCTCACC 300 AAGTTGGGGC TTTGTCTATT TACCGTTGTG TTCCCAGTGG ACACTCGATG TTAAGATTCA 360 ACGAATGAAT GCCTGGACGA GTGGTATCTG GGCTCACAGG TAACCTCACA GCCCACCGGG 420 AGGACACTGC CAGAGCTGCT CTGCACTGCG AGTCCCGGGC CTTCCCATTG GACGCTAAGG 480 CACTCGTTAA CTGCTGTGTA AACGCAGCCT GACTTCCCTC ACCTCAGGCG AGGCCCGCAT 540 CAGGCCCCTC TGACCTAGGA CCTCCCGATC CGGCCGTTAT CGCCAACCGT ATCTGTGTGG 600 TTTCGTGGAG GAAGCGCGGT GGACCTTGAG GGGAGGGTAC GCGCAGGCAC AATAAAGCAG 660 AAAGCCGCTA TAATAATGAT GATAATGAAG AAAAACAAAA GCATCCATTC GTCACTTAGT 720 GGCAAGCGTT TTTCCAACTA CTTTCCGAGT AGTAACTGCT TGCCAGAGTT TCCCCAGCTT 780 GGGCCGGAAG GTGAGGCGGT AGCTCGAGCT TTGCCTTTCT CAGGCATTGT CCTGCGTTTG 840 CGGGGCCAGG CGCTGGCACA CGGTCACTAA CCCCTGGTCG TTAGCTTCGA TTCCCGGCCT 900 GGGAGAGCGC TATCGGCCAC TCCTGGCTGC ATTGCAGTCG CGGCTTTCTC CAGAGCTCCG 960 CCGGGAACGG GAAGCGCTGA AACGTCGCGA CCAGTCAGTA GGGTTCCCAC GGCCGCAACT 1020 CGGGTGTGAC GCGGCAGGCT GGCACCAGCG GACACAAGTA TGAGGCTAAG TGAGAAGCGC 1080 TCTGCTTCCG AGTGTCAGGA TGGCCGAGTG GTCTAAGGCG CCAGACTCAA GGTAAGCACC 1140 TTGCCTGCGG GCTTTCTGGT CTCCGGATGG AGGCGTGGGT TCGAATCCCA CTTCTGACAC 1200 ATTCGTTTTA TTAGCATTTT ATTCCCCGGA AGAAACCCCA GAATTTTCCC GGAGTCCGTT 1260 GGTATTTTAT TGTCTTCTCC AGGAAGAAGG TTACAACTAG ACTACTCATC TTTGCTGCCC 1320 GGTTTTCCCT GTCTGCCGCA GCAAGGGGGC TACCTACCAA GGGGAGGGAA GCAGTCTGCA 1380 TATTCCCAAA TGTTGCGAGA AAACCGCATC CAATCATGTT TCTATAGGAG ATACGTCACA 1440 GGATATTTAT TTAGTATAGC ATATTGCTAA ATGACGCATC 1480
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