Tag | Content |
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EnhancerAtlas ID | HS040-21686 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr2:241790420-241791270 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr2:241790893-241790908 | TGACCTCTGACCCCA | - | 7.91 | Nr2f6 | MA0677.1 | chr2:241790893-241790907 | TGACCTCTGACCCC | - | 7.03 | Rxra | MA0512.2 | chr2:241790893-241790907 | TGACCTCTGACCCC | - | 6.98 | Zfx | MA0146.2 | chr2:241790605-241790619 | CAGGCCCAGGCGGG | - | 6.37 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I240851 | chr2 | 241790721 | 241790890 |
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Enhancer Sequence | AAGCCTCCAC CAGCCCTGGC CCGCTGGCTG GGTCCCTCCC CGAGAGCCAG GTCACCTGTC 60 ACTGTCTCTC ACCATCCTCA GCCCCATGGA CTGTGCTGCA GGTGGCCACT GTCACGTCAC 120 CCAGGCCAAG CACACCCGTC AGGATTCCCA AGGCAGGTCG GTGTCCAGCC GCTTCCCTGA 180 GGCTGCAGGC CCAGGCGGGC TGCGGAGTCT GTGCCTACAT ACCGCGGGCC GAGCTTGCTC 240 CAGGCAGGGA CGGCGCGGGA GGCACAGGTC CTCTTTGGGC CTTTCTGCAG GTCCTCCTGC 300 CCCACATGGA CATGCCAGCT GTCACTTGCA CCATCAGGAA GAACAAGAAT CCTGTGTGCC 360 CTGTGGTGGG GCCACAGTCG GCCGCTAGGT GTCACTGTTT CCTCAGAGAC CAGCACATTG 420 TCCCTATGCT TTCTCTCTGC AGTCCCTGGC TGGCAGCTCC TTGGGCAGGG TGGTGACCTC 480 TGACCCCAGA CCCGTCCCCC CTGAGCTGGT CCTGGCTCCA CCGGGAGCTC CGTCCCCTGG 540 GCTTCCTGCT GATATGTAAG TCAAGCCTGA GCTGCCGCGT TGGGGCCACT GATCTGGGCA 600 GAGCCTCGTG GGGTCTCCCA GGGGCTCAGA CGTTGGCCAG GACCCCACAG GGAGGATGCT 660 CAGGTCAAAA AGATGCCCGC ACTCCGGGCG CTGCCCAGAG CTCTTAACTC TCATGCTGAG 720 AACAGCTTTG TGTGCTGAGT GTTTCGCACA CCCGCAGGCC CCGCACGTTC TGCCTGCTGT 780 TCCCTGTAAT CCTGACCTCG CCTGGGAGTG GCAGGGCCAC CCACTTCGGG AGCGGTGGAG 840 ATTGGACTAT 850
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