| Tag | Content |
|---|
EnhancerAtlas ID | HS040-15080 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr17:26840580-26842030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2A | MA0003.3 | chr17:26841536-26841547 | AGCCTCAGGCA | + | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27527 | chr17:26840484-26842450 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I028513 | chr17 | 26840485 | 26842450 |
|
Enhancer Sequence | GGCCTCCCCA GGGCTGCTAG GAAGGGCCTG TGGTCCTGTG GCATTTATGG GGCATGTGAC 60
CTGCCTGCCT GGCCTGGGGA GACAGCCCCG CCTCAGCCCT CGGGCAGGGG GCCGGTCCAG 120
GCATGTGGGA GTATTTATAC CTCGATGGAG GCTCCTGGGG AGCTGCAGGC TGAATGACTC 180
CCCGAAGCGG TGATGGTGGC CATGACCCAG AGCCCACTGT GAGTGCTTGG ATTTGGCTCC 240
TTTGGGGCCA TGGCTGGGTG GCAGAGGTTA GAGAGGGGCT GGAGAGACGG GAAGGTGCCC 300
AGAGGCAGCC AGGGATGGCG AAAAGGAAGG GGTGCTGGGC AAAGGAGAGT GGGAGACTGG 360
TTGCTGTTGG AGTCAGGCAT CTGAAGCAAA GCTGGGACCC TCCCTGCAGA AGGGATGAGT 420
CTATTGCCCT TAAAGAGGCT CTGGTGGGTG GCTTGGTGAA TGGCAGGAAG GACAGGACAA 480
GAGGACTAAG ATTACAATAA ATAGGGATTA GAGATCTGGA AGAACCTCCA GGTCGGCCCA 540
AGGCTCAAGT GCTTTTCCAG GATGGGCGTA CTAGGCAATG CTCTGGGACC AGCCTGCTTC 600
CAGAGGCACA TGGGAATGCT GAAGAGTCTT TAGGAGAAGC CTGATTTGGG GACTGGAATG 660
ACTCAGCTGC AGGTGTCGGT GGCTCACATG GAGGAAAGCG TCACCTGGGG GACATGGTGG 720
CTTTTCATCC TTTGTTCTCC CCACTCCCCT CCCTGCCCAT TCTGTCCCTA CCTGCTCTGT 780
ACTTGAGTCA GATCTCAAGG CAGGGGCACG CAACCCATTT TCCGAAACTG ATGCTGGGTT 840
AAGAGCCAGG GAGGCCAGAA TTTTGCCCTC AGAACTTCCA ACATTGATGG GGAGAAAGGA 900
GCTAGAAACC CCCTCTTTCT TGGCATTCCC AGACCCCGAG TTTCCTTGGG TGCCCAAGCC 960
TCAGGCAGAG CCCCCAGGTC CTTCCCTGCC ACCCCCATAA TTGCCGAGCT GCTCCAGGGG 1020
ACCCCTCCCA GCAGCCTGTC GGGTGGAGCC CTGGGTGGGG CTACAGGCCA GCACCCGGCC 1080
GGCCGAGCCC CACCCCTCGT AAAACATGCT GCCGCAGCCA GCAACAGAAA CCATTAAGGT 1140
GGAACTGAGC CGTCCCCACC TCACTCATAA AGAGTGGGTA GGAGGCCGCC AGGTGGGAGG 1200
CAGCAGGGAG CGTGAAGAGA GCCTGGGGAG GACCCTTGGT GCCCCAGGCC TGTCTGTCCC 1260
TGTGATTCAG TTGCCCACAG GGGAGGCAGG GACAGACCCT CCCAAGGAAA CCTCCAACGT 1320
CGCCCCCACC CACCTTTCAG GCTTGAGCAG GGAGGCTGAG GCGTTACCAA GGTGGGGCCG 1380
TGTAGCGTAA TGGTTCAGCA TGCTGGCTTT GAAGCCCGGG TTGGAATCCT GGGGAGCATA 1440
ATATACTAGC 1450
|
