| Tag | Content |
|---|
EnhancerAtlas ID | HS184-31777 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr9:135627940-135629390 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr9:135628004-135628015 | CCACACCCTGC | + | 6.62 | | RREB1 | MA0073.1 | chr9:135628105-135628125 | CCCCCACCCACCCCACCTGC | + | 6.78 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr9 | 135628233 | 135628449 | | chr9 | 135628028 | 135628097 | | chr9 | 135628182 | 135628718 |
| Enhancer Sequence | TTTCTAACTT TTCTACAATA AGTAGATGCC CTGTGTAATC AAATGTTTGA AATAACCACC 60
TTCGCCACAC CCTGCCCCCA CCTTGTTCCT CCAGTGGCTT CCCTTCCCCC AGCTCTCCTG 120
GAATGGGCCT GGCTGTCCCT GGCCCAGGAC ATGGACGCTG GCTGCCCCCC ACCCACCCCA 180
CCTGCAGAAC TCTTCCTCCC CTCCTCCTGC AGCTGGCTCC TTCCTTCCAT TCAAGTCTGA 240
GCTTAAACCA GCCCTCCTCA GAGGCACCTT CCCCCACCAG CGCATCCAAA CCAGTCAGCT 300
TGCCCCTACT CCATCATGCC ATGGCATTTT AATCCCACAT AAAGCACTTG GTCCTAGCAG 360
GTATTTCTGC TCTGTTTATT TGTCTAACGT CGCCTCCTCC CATGGGAATG TTTTGCTTGT 420
TTCTGTGGCC CCAGCGTCTG GAACGGTGCC TGGCAAAGAG AAGCCTACAA TAAATACTTC 480
TGGAGCGAAC AAATTGAAGT GTAAGTCCTT CCCTTACTAC TAGGAATAGC AGCTGCCACA 540
ACTGGGCTCC GAGCTGATCA TTCTACACTG GGGAATCACG CCGCATTCCC AGGAGGAAGG 600
AGCCAGGCCA CTGTTGACCT CCTTTTGTCC TGGGGAATCT GAGGATCAGA GACATAAAGT 660
AACCTCCCTG TCACCCCCCT AGTAAGCCAG CTGGTTCTGG GCTCTCTCAT CTTGCCGCTC 720
CACTGCCAAG AACAACCTCC ATCCTATGCT AGGGGCTGGG CCTGGCCCTG CAGGATGTGG 780
GCCTGGCTGG CAGGCAGCCC TGACCCTCTG CCTGGCCCCA GTGGCAGGGT CCCCACAACT 840
CCTATCTGGG AAGGGCTTAG GGGCAGCAGC CCAGTTAGAA CTGCTCATTG GACATGTTCA 900
CAAAGCTGCA CACACTGTTT ACTGAGACGA TGGCTTTATT TGGGGTGGCT GGGGCAGAGA 960
GAGCTCATGA GTGTGGGGGC TGAAGCCATC CCTGGACTAA TCCCCAGGTA CTCACATCCT 1020
GGTAGGGAAG GGCCCCTGGC ACAGGCTCAG GCTGGTGGCT TTAAGCCAGT TTCCTTGCTG 1080
GAGGGTATGG GTCATCCCCA GGGTGGCCCA GCTGGGGCGG AAGGGCACCC TCGCAGTGAG 1140
GGGATCCCCG CTGTGGAGAG CATGAAGCCC CTCCATGTTC TCTAGGGAAG GAGACAAGTG 1200
GGCAGGAGAC AAGTGCTCTC ACGCCCCATC CCTGCAGCCT CCTGGAGTGG CACGCAGGTG 1260
ACAATGGGGA CTGCAGGGAG CATGCACGAA GGTCTCCTCT TCGTATTTAC TCATCCAGTC 1320
TTTCCACTGC CGTCTGAATT AGGTCCCATC ATTGCCTCCA TTTTATGATG CAGAAGGAGC 1380
CCTCCAGGTG GGATAAGTCA TTCAGACAGC GCAACTCACA GAGGGCACTG GAGCCCGGAG 1440
TGCGGTTCCA 1450
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