Tag | Content |
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EnhancerAtlas ID | HS012-19936 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr5:94598520-94599890 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr5:94598811-94598826 | AAGGTCCAGAGTTCA | + | 6.32 | SP8 | MA0747.1 | chr5:94599208-94599220 | CCCACGCCCACT | + | 6.14 |
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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 |
GH05I095262 | chr5 | 94598340 | 94599249 |
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Enhancer Sequence | TATGTCAAAC AATGTCATCT ATCCCTAATT ATTCTATATA CTACATTAAA AATTAAAAGC 60 TTTTTTCAAT CAGTAGACAA ATCATATATT TGTTATTCAA TTTGATTTCG CATTATGGGG 120 CATTTACTAT GTGCAAAGCA TATATGAAGC AAAGGGAGTG ACTACAAGTG ACTCCTGCTT 180 AGACCTTCCA TTTTAAGATG TGACAGAAAA ATTGTGCAAG TGTACGAAGG CTAAGCCTTA 240 TGAAAACATT ATCTATGCAG TGCAAGCAGT CTCTGGCTTC CTGAACTGGG GAAGGTCCAG 300 AGTTCACTAG GAAGCTATGT TTACTGGCTT CATTTGCCCA GAGAAGCAAT GTCACTAATG 360 GGAGTTGGTT TCCAGATGAG ACCTCCTAAT GTACTTCTAG CAGCTCCAGC CCAAGTTCTG 420 AGAGCAAGAA ATCATGAGGG ACAGGACGGT GGCAGAGGAG AACAGGGCAG TTTCCCATTC 480 CCTTGCCAGA CCCAGAGCCA TTCTTCAGCC AAGCTATGGA TCAAAGCAAG TCTGTAGTTA 540 GCATCTCATG CCTCCCTTCC CATGCACCTC CATTCAAAGC TCCACTAGTT TCCAGCCTCT 600 TGTCACCTCC CCCATACTAA GTCCTGTGGC ACCCATCCAG GCCCAGGTTG CTGCCACAAA 660 TTCTACAGAT TGAGCTAAAT CACTCTCACC CACGCCCACT GCTCAAAATT TACAATGTTC 720 TATCCAGAAA TTAGAAGGCA AGAACCTAGC TGAGTTAATT CATGCTAAAG TATAAATGGT 780 CATTCCTGAA GGCTCCAAGA GACACCAGTA TAACTTTTAA AGATACCTGC TGCCTCAAAA 840 GTGGAGATGA ACGACTATCA GAAGTGATGG AGTGGAGGAG AATAAAGAAT GTGTATTGAG 900 CATTGCCATG TGCCAGGAAC TTTCATTGTA CCCTCCTAAC AGCACCATCA GGTTGGTATG 960 TTATTCCCCC AGATTTACAG AAAAGAAATG TGAGGTTTAG AGAGGTTAAG ACTTACTCAA 1020 GCTCTGGAAG ACAGTCTGCC TCCACCTCTC TTCCCCATGG GCAAAGTCAA CCAGTCCAGT 1080 CTCCACCCAG GGGCAGGCAA CTCTCCTAGG CCATTCTTCC CTTGCACTGT TTCTTCTCTT 1140 CCTTTGTATT GAAACCACAG ATCCCCTTAA AAAACCATCT TCTTGCAAAG TGTGATGACA 1200 GGGACAGTAA AAGAAGCTGA GGCAGCAATG GGTAAACACT ACTAAAGCAT ATTTGTATAA 1260 TGAAGCTGCT TGCAAGTGGA GTGTGGATCA GGAACTGCTT ATATTCTAGG CTCTGAAAGG 1320 AGGAAAAGAG GATGGTAAGT GGATTTATCC CTTGAGCGTC AGTATCTACC 1370
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