Tag | Content |
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EnhancerAtlas ID | HS101-19441 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr17:71355560-71356820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EN2 | MA0642.1 | chr17:71356519-71356529 | GCTAATTGGG | - | 6.02 | KLF5 | MA0599.1 | chr17:71356316-71356326 | GGGGCGGGGC | - | 6.02 | ZNF263 | MA0528.1 | chr17:71356766-71356787 | GGGGAAGGGAGGTGAAGAGGA | + | 6.36 | ZNF263 | MA0528.1 | chr17:71356748-71356769 | GGGGGATGAGGGGTGGGAGGG | + | 6.52 | ZNF263 | MA0528.1 | chr17:71356751-71356772 | GGATGAGGGGTGGGAGGGGAA | + | 7 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_69033 | chr17:71355908-71358370 | H9 |
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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 |
GH17I073359 | chr17 | 71356032 | 71357670 |
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Enhancer Sequence | GAGTAACTGC GGGGTCAGGT GGGGTGGACA CGCCTGAGGG AGTATGGTAG GGCAGGCAGC 60 CCTCAGGACC CTGTACTCAT CCTGCACAGG ACAGTACTCA GGGCTGAGGA CAGAGCCTGC 120 ACCTTCTCCG GGGCCAGGAG CTTCCAGCGA GTCCAGCCAC TGCCTGGCTG CATGTTCCCC 180 GCCTGCAGAC CGCCCCCTGC ACCCACACCA TGTGGGAGGA TGGCTTCTTT ATTTCTTTTT 240 TTGAGACACG TTCTCACTCT GTTGCCCAGG CGGGAGTGCA GGGGCACGAT CACAGCTCAC 300 TGCAGCCTCC ACCTCCTGGG CTCAAACGAT TCTCCCACGA CAGCCTCCTG AGTAGCTGGG 360 ACTTCAGGTA TTCACCAGTA TGCCTGGATA ATTTTATTTT TGTAGAGATG GGGTTTTGCT 420 GTATTGCCCA GGCTGGTCTT GAACTCCTGG GCTCAGGCAA TCCACCCGCC TCCACCTCCC 480 AAAATGTTGG GATTACAGGC GTGAACCCCC ACACCCGGCT GGTTCTTTCT TTCTCAGAGT 540 GCCCTCCACT ACCTTCTCTG AACCCTCTGC CCTTTATCTC CTCCCACCTC CCCACCTCTC 600 AGCCTGGGAC ACTTCAAGCC TCAGGATAGA ACAGCCTGTC CTCCGCACAG CCCTCTCCTG 660 TCCCCAGGCC ACTGCCAACG CTTGGTCCTC AGTTGCTTGC CAGCTCTCTC TCCTACTTTT 720 GTTTCCCAGG AAGCTGGCTC AGGTGAGAGG CAGCGCGGGG CGGGGCTGGA GGCAGATGAA 780 AGGACAGCGG CTGGGTGGCT CCTGGGCTGC CTCCTGCAGG CTTTGTCCTG AGTTTGCCCT 840 AGAGCTACAG GGCTTCTTTG CAGAACCAGA CTGTGGGGAA TAGAAAGTGA CTGGCCAGAA 900 AGAAAAAGTG AAGCGCAGCC AGACTAAGCC ATTAGGGGAA GACTCTCTTC CTGAGTCAGG 960 CTAATTGGGA CTGCTGGGGA GGGGAGGCCT GCGCCATTCT TGGCTGAAGG GGGTGGGCAG 1020 AGGAGGAGAT GGGATTTTAG GGGAAGTCCA GGATGGGCTG TACCCCTTCT TAGGGAGGGA 1080 GGCAGCAGAG TGGTCTGGGA GGTGACTTTT GTGTTCAGGA CAGGACATTC TACACTGACC 1140 AGTAACAGGG ACTTTGGAGG GCTAAACCTT GACCATGGCA AATGCCTGGG GGGATGAGGG 1200 GTGGGAGGGG AAGGGAGGTG AAGAGGACAT TTAAAGGAGG CGATTGGGCA CAGTGGCTCA 1260
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