Tag | Content |
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EnhancerAtlas ID | HS101-46385 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr9:131964640-131965950 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr9:131965441-131965451 | GGGGCGGGGC | - | 6.02 | SP2 | MA0516.2 | chr9:131965438-131965455 | TAAGGGGCGGGGCTGGG | - | 6.08 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_53874 | chr9:131964865-131965891 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 131964929 | 131965182 | chr9 | 131965304 | 131965800 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I129202 | chr9 | 131964601 | 131966079 |
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Enhancer Sequence | TCTGGGCCAA TTTCCTCATC GGTATAATGA AGGGGTTGGC AGGGCTAGTT CTGAATTTTC 60 CCAACCCACC CATAAAATTC ACCCTTCAAA TTCTAAAGAT TCCATTCCGT GGTCTAACTC 120 TGTGTGTCTG TCCTTGGTTC CAAAAGTCCC CGTCCTTGTG GCCCCTGTTG TTTTGGACCC 180 ATCACAGGTA ATTATGTATT TGTGTGATTA AACATCCCTG GCCTGTCTCC CTGCCTGGGC 240 TGTGTGCTCA GCAAAGAACC ATGCCTGTCT CTGTCTTTGT CCTTTAAGAG ATCAGCACAG 300 GGCCTAGCGC ATAGTAGGTG CTCACTAAAT ACTGTAGCAG CTGGTATTGT TGGGAAATGA 360 TGCTGGGAGA GGCTGCTGCT GGAGAGAAGG GAGCCACCGA CCGCCCTGCA GGCAGTCAGC 420 GCCCTCAGTC CCTTCCTCCT CGCGGGCCGC AGAGGCTCCC CTTTCCCCGA GACGATAAGA 480 ATGCCCAGAC GCCCCAAAAC CCAGGCCGCG CCCCTCCGGG TAGAACTACA GTCCCCAGAA 540 GGCCGCGAGG GGCGGAGCCA CCAGCGCCCG CCCCGCCCGG GCCCGCCATG CCGCACAGCA 600 TCATGGGAGT TGTAGTTCAG GCCCTGTCCC CCGGGCAGCC GCTGGCGCGG ACGTTCGCGG 660 AGCAGCCCGG CGCCCGCGCG GCTCACGGGG CCCTAGGACC CCTCCCCTGG GGGACCTCCA 720 CCCTCCGCAG GCCTTTTGAA TTAATCCTAC TGCGCCGGGG ACCCCAGGAC AGTTCTGTCG 780 CGTACTCCCG GGACCCTTTA AGGGGCGGGG CTGGGATCCT GCCCCACCCT TGACTCCCCC 840 ACCCTCCTCT CTCAAACATC ACCCCGGGCG CTTTAAAACG CTTGATCTCG CTGGAACCTT 900 TTCGGTCTCC GTTAGCCACA CCTTGATTGT CGAGTGTGTG TCTGGCCCTT TGGGGACAGC 960 GCTTAAAGTC GGGGTGGGCG GGGGAGGGGA TCACCGACAT TCAGTCTTGA GTGACACACC 1020 AGATGACCCC ACCGGAGAGG AGGAGGGTGG CACAGGGGCC TGACGGACCT GGGGTATGGG 1080 CAAGGCTTCC AGGGGCCGGT GACATTCAGA CTAGGCCTGG GTTGGCCAGG GCAGGAGCAG 1140 GGAAGGGTGT TCCAGTCAGA GGGAACAGCA TGAAGGAGGG CTTCGAGGCT TTAGGGGAAG 1200 CAAAAGAAGG CCTGGGAGGC TGGCAGGCAG AGAACGGCTG GGGAGGGGCC GCTGGGAGGG 1260 GTGGAGAGGT GAGTAGGGCC CGTGGGAAGC ACCTGGCGAA GAGTGTTTCT 1310
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