Tag | Content |
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EnhancerAtlas ID | HS040-00014 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:1094700-1095120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF3 | MA0522.2 | chr1:1094892-1094902 | AGCAGGTGTT | - | 6.02 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_23183 | chr1:1092822-1104598 | Colon_Crypt_1 | SE_23779 | chr1:1092838-1103486 | Colon_Crypt_2 | SE_24694 | chr1:1092804-1107737 | Colon_Crypt_3 | SE_28002 | chr1:1092840-1096046 | Fetal_Intestine | SE_29232 | chr1:1092782-1095755 | Fetal_Intestine_Large | SE_31594 | chr1:1090819-1107666 | Gastric | SE_34473 | chr1:1092829-1094897 | HCT-116 | SE_34473 | chr1:1094950-1095618 | HCT-116 | SE_50578 | chr1:1092807-1104591 | Sigmoid_Colon | SE_52392 | chr1:1092813-1096108 | Small_Intestine | SE_56870 | chr1:1094646-1095408 | VACO_400 | SE_57937 | chr1:1094647-1095384 | VACO_9m |
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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 |
GH01I001156 | chr1 | 1091598 | 1096031 |
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Enhancer Sequence | CATTTAAAAA AAGAAAAGCA GGTGAGGACG TGTGAGCAAG TCTGGGCCAT GCTGCCAAGC 60 TCCCGCTTCT CCGAGCAGCT CCACACAAGG AGCAGAGGCA GCTCCAGTTC CACAGCCAGA 120 CACAGTCATT TTCCCTCTAC TCAGGAATTA GGCAGGATGG TGTGGGGCCT GAGTGTCACC 180 ATGAAGCCGG GAAGCAGGTG TTCAGCCAGA CGCAAATATT CCTCCTCAAA GCCAGGGGAG 240 CGGCCACAGT GGATTTTATT ATGGGGCGAC GGGGGCACGC CCAGTGCCCC GCCACTCTCC 300 ATGTCCACAG CAGCGAGGGT GGAGGGCCCT GTGCTGTGCA GGGCAGAGCT CGGCTGCACC 360 TGGGCCAGGA CACAGCTGCC CAGGTGGGAG GAACCGTGGA CGGGGCTGGG GCCTTCCTCG 420
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