Tag | Content |
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EnhancerAtlas ID | HS048-14813 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr16:81437040-81437910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr16:81437292-81437303 | AGGCCATAAAA | + | 6.02 | CTCF | MA0139.1 | chr16:81437304-81437323 | CGTCCAGCAGAGGGCGCCC | + | 7.3 |
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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 |
GH16I081403 | chr16 | 81436774 | 81441457 |
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Enhancer Sequence | TATTGTGGGA TCAATGAATT CTAAATAAAA AATGCACTAA AAGTCTGTAG TGGGTGATGG 60 GGTGGGGGAT TTAGGGGTGC CGACGGGGTA GACCCCTATT GAAAGAGGCA CGAAAACTGG 120 GAGATGAAAA GCATAGGCTC GTTTGCCCTG TGTCTTCCTT CTCACGGCAG GGGATCGGCC 180 GGCCACCTTC TCCCTGTGAC TTCCTCCCAG TCCCGTCACC AAACCCCTGA GGCCGTCCTG 240 GCATCAGACC GCAGGCCATA AAAGCGTCCA GCAGAGGGCG CCCCAAACCC ACGAGGGCCG 300 CGGCGAAGAA GAAGGTAGCG GCCGCTGTCC TCTCCCCTCC CAGGCAGGTC CGGTGCGGAA 360 GGGATCGCTG GACACTGGCG ATGGTGGAGA GGCATGGTGG GCCGGGTCCC CCGCACCCTT 420 CATGGCCCTG ACTCGGGGCT GCCCATGACC TTCAGCGTCA GAGCTCGGTC TGGTCCATGC 480 CTGCCTTGGG GAAGCTGCGC CGCCTCTGCA CCCACCCAGG TCAGGGCCAC CTTCCCTCCA 540 TTTGCAGCAT GAGCAGGTCT GAGGTGGCGG CTCCGGGCTG AACAGCAGGA ACTGAGTTCT 600 TTGTCCACAT GTGAGGGTGG GCAGCCCATG AACAGTCCAC CCAGACACAA GTTACCCTGC 660 CCCCGAGCCG GAATCCAGCC CTGAGACCCC ACAGTGCTGC CTCTGAAACA GTGCTGGGAC 720 GTCTCTCTGA GCCTGAGCTC AGACTTTGGT GTCCCGCTGC TGAGGCCGGG GTCCCGCCGC 780 TGTGACCGTG GCAAGGGTAA GCCCTTTGTG CACCTGTGCC GTTGCCTGTA AAATGCTGGC 840 AGTAATCACA GTGGAGCTAC CCTAGAGGTT 870
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