Tag | Content |
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EnhancerAtlas ID | HS040-16463 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr17:79045480-79046600 |
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) |
TFAP2C | MA0524.2 | chr17:79046020-79046032 | TGCCCCAGGGCA | - | 6.44 | TFAP2C | MA0524.2 | chr17:79046020-79046032 | TGCCCCAGGGCA | + | 7.22 | ZNF263 | MA0528.1 | chr17:79045777-79045798 | CCCCCCCTCCCCCTCTGCTTC | - | 6.49 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_25200 | chr17:79044943-79047388 | Colon_Crypt_3 | SE_26560 | chr17:79045419-79046435 | Esophagus | SE_31420 | chr17:79036752-79047540 | Gastric | SE_34261 | chr17:79045234-79046799 | HCT-116 | SE_42160 | chr17:79042160-79048985 | Lung | SE_57453 | chr17:79043992-79047414 | VACO_503 | SE_57915 | chr17:79046004-79046370 | VACO_9m | SE_65309 | chr17:79045618-79046726 | Pancreatic_islets |
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| 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 |
GH17I081071 | chr17 | 79044984 | 79046933 |
|
Enhancer Sequence | GCCTCTGTTT GAGGGACTCA CGTCCAGCTC CCGGCAGACT CAGCGCGGGG GTCGGATGCC 60 TTCTCCGCAC CATCCCGCAC CGCCACGAGC TGCTGTGGCT CACATTCTGC CATCCGAGCT 120 CTGTCCAGGA GGCAGCCGAG AATTGGAGCA GTTCCCACGC CAAGTAGGGC CTTGTGGGTG 180 GCCGGTCCCC TCCTCCAGCG TGGCACGGAG GCGCCGGAGC ATGCAGGTCT ATGCCTCTGC 240 AGAGTCTGGG GCATCTTGTT CCATTTCCTT GCTGCCTCTC CTCTCGTCCG TGATCATCCC 300 CCCCTCCCCC TCTGCTTCCG GCCTCCCCGG CCTTCCCAGT CTCTTGGGCC ATCATCGTGG 360 TTGTGTTGGT CCTGTTGCTC CTCCTTCGAG CGCCCACGTA GGGCTGGGGT TCCCTGCGGG 420 CTGTGGGTGC CGTGCCCTCC CCGGCTGGCT CCAGCCCTCA GAAGCTTGGG GAGGGTGGGC 480 TGGGCCATCT GCATTCCACC TGCCCAAGGG CTGCCACTCC CTTTTCCCAG ATGGCTGGAG 540 TGCCCCAGGG CAGCGTTGGG AGACCTGCGC AGGCCCCACC TCAGTCCACA ACAATGTTCC 600 TTGATTCCCT CCGGCTTCCT GCTCCTTCAC CTCCTCCTGC GCAGCCCGGC CTGACCCATG 660 TAATCAGGGA ACAGGAGGGG CTCTCCTCAG TGTCCCTATG TCCATGCCTT GTGGCCACCT 720 GAGCACTTCT CAGGGTCCAG TGGAAAACTC TCCTGCCCTG TTTGACGCCC ACACTCGTCA 780 GTTTCACCTT GGTGCCAAGA GCAGACGATC TGCTCCAGGC CCCACTTGGG CCACAGCCTC 840 ACAGCCGTCT CCACGTCCCC ACCCGAACCT GGCATTTCCT GAATTCCTGG CCCCTGTCCG 900 AGAAGGAGGC TAACCCTCCT GGGAGAGCTC TGGCAGGTGC TGACCCAAGT CCGTGGGGTC 960 TTCAACCTTT GCAGACACCT GCGCCCAGAG GCCACGCCTC CCACTCTGAG CACAGGCGGG 1020 CGGACGCTGT CTGGCAGGCT CTGCCTTTCT TTCATTTTTC CTGACCTCTT CGCCCAGCGT 1080 CCTCTGCTTG GAGGTGGGTG TATGAGAAGG GGCCATTGGT 1120
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