Tag | Content |
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EnhancerAtlas ID | HS012-15517 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr19:33769220-33770320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr19:33769287-33769308 | TTTTTCTTTCTTTTTTTCTTT | + | 6.67 | SP2 | MA0516.2 | chr19:33769821-33769838 | GCAAGCCCCCCCCACCC | + | 6.04 | ZNF740 | MA0753.2 | chr19:33769823-33769836 | AAGCCCCCCCCAC | + | 6.2 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_24807 | chr19:33769329-33770181 | Colon_Crypt_3 | SE_35421 | chr19:33764588-33771627 | HepG2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 33769544 | 33769942 | chr19 | 33769918 | 33770040 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I033277 | chr19 | 33768840 | 33771906 |
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Enhancer Sequence | TCTTCCTCTC CGTGCCTTGC TTTTGGACTT TCAGGCCACA TCACATTCCT TTTTCTTTTC 60 TTTTCTTTTT TTCTTTCTTT TTTTCTTTTT TTTGTAGAGA TGGGGTCTTG CTATGTTGCC 120 CAGGCTGACC TCCAACCCCT GGCCTCAAGG GATCCTCCTG CCTCAGCCTT CTAAAGTGCT 180 GGGATGACTC TGACTCTTTC TCTGCTTCCT CCTGTCTCTG TTGGTCCCAG TTTCTGTCTC 240 TCTAGGGGGG CATCCCAGGA GAGGGGCAAG GTTCAGGCCT CAGGGCTTAA GCCCCTTGGC 300 TGCTGGGCCA GGCCTTCCTC TTTCTGCTGT CTGTCCCCTG CCCTGCTTCC TTACTCTGGC 360 CAGAGCCGAC TTGCCCTTTG CCCTGGAGCT GCGGCACCTC GGGGTTGGGG GAACTGATGG 420 CCTCACCTCC CCCACCCCCT GCAGCCCCTG CTCCTCCCCA CAGGAGTCTG GCCAGAGAGT 480 TGGGCCCTGG GGAGGCCACA CAGCCAGGAC ACATGTCCTG GCCCCAGGCA GAACCCTTGC 540 CCTGGCCACA GAGCCACACC AGCCAGGTCA ACTCTGTCCT CTGAAATCCC TGGAGACCAG 600 GGCAAGCCCC CCCCACCCAC TCCCTGGGGC AGCTTCGGAC TCCCACTCAC CTCCAGGTTG 660 GGAAAACTGA CCCCCAGCCC AGGGCAGGAG GCAGGATGTG GAAGGGCCTC TAGCAGAGCT 720 GAGGTCCAGC CGGCCATGTC GGGGGAAGGA CGACCCTGTA CCCTGTCATT CCCCTCACAG 780 TGTGAGGCCC CAGGGAATAA CCTGCCCTGG CAGGGGACTG AGAAGCAGGA GCAGTTTCCC 840 AGCTCTGGAG CATGCTGGGT GGGAGCAGGC ACGGGGCGTC TCTGGGGGTG GGGAGCAGCC 900 CCTCCTTGCC TAGGCAGTCA CTTTCTGGGG GCCAGCACTT CCCACACTCT CTTTTTTTTT 960 TTTGAGACAG AGTCTCACTT TGTCACCCAG GCTGGAGTGC AGTGGCACGA CCTCGGCTCG 1020 CTGCAACTTC CACCTCCTGG GTTCAAGCAA TTCTCCAGCC TCAGCCTCCC AAGTAGCTAG 1080 GATTACAGGC GTGTGCCACC 1100
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