Tag | Content |
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EnhancerAtlas ID | HS040-18660 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr19:45615750-45616520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr19:45615846-45615865 | CCCTGCCCTCTAGTGGCCA | - | 7.29 |
|
| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_24339 | chr19:45615643-45617982 | Colon_Crypt_2 | SE_27949 | chr19:45615350-45618138 | Fetal_Intestine | SE_28778 | chr19:45615454-45618106 | Fetal_Intestine_Large | SE_31565 | chr19:45615415-45618886 | Gastric | SE_50849 | chr19:45615743-45617589 | Sigmoid_Colon | SE_53046 | chr19:45615648-45617960 | Small_Intestine | SE_65319 | chr19:45615291-45623609 | Pancreatic_islets |
|
| 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 |
GH19I045112 | chr19 | 45615504 | 45617954 |
|
Enhancer Sequence | CCTGGCTGTC TTTCCTTCAG CACCTACTTA GGGGAGCAGC AGCTGTGTGC CTAGTGTAGT 60 TATGTTCTGG GGGGCAATGC GAACAAGACT CACAGTCCCT GCCCTCTAGT GGCCAGTGGT 120 GTTAGATGGT CCCTCTTTCA GGACGCCCCC AACCCCAAGT CTGGGTTAGG GGTTTCCTTT 180 GCCCCAGCTC TACCTACTCT GGCTTGTCAC TGTCTAGGGA TGGGTCTGCC TTCCCGACTG 240 GACCAGGACT CCTGTGTGGA CAGAGACCAG GATTAGGGTT GTCTTGGACG CTGTTTCCAG 300 CATGACCCTG CCCGGGGCAC AGAGCAGGTG CTGGGTGAAG CAGGTGCTGG GTGAAGCAGG 360 TACTGTTGAG CTTGAGGCAG TTGGGGTCAA GAGGAAGAAA TGGATTCTAG TATCCAGGAC 420 TTTCTGGAGT AGGACCTGGA CCCCAAGGCC ATGTAAGCCC AAAGCCTCAT ACTTTCCCTA 480 ATGCCTGAGT GTTCAAGATT CCTTTACCTG TGCTGGGCTC TGTGGCAGAG GGAGGGGTCA 540 CAGCTCCTGC CCTCGACAGC TTAGAGAAGA GTCAGTGCCT AACTACACAC CCCTTCCATA 600 GTGTGCAGGG CTGGGGATGT GCGGCTGGCA GGGTCCTCAC AGAGAAATGT GAAGCCCACC 660 CGGCCCTCTG GGAGCTCAAG TGTTGGCATG TCTTTTCTGA AGAGGGTGAG GGCAGGAAGA 720 TGTGCATTAC CCTTAGAAAA AAAGTAGAAA AGGCCAGCCT TCTCATGCAG 770
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