| Tag | Content |
|---|
EnhancerAtlas ID | HS115-03176 | Organism | Homo sapiens | Tissue/cell | Kidney_cortex | Coordinate | chr4:9692050-9693460 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr4:9693307-9693317 | GCCCCGCCCC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGACTGAGAG GGTATATGCA ATATCTCAGA CCCAGAAACC GTTGATTCTG TCTAAAAGCA 60
CAGCAATAAC CACATCCCAC CCTCTTGATT TAAATGAAAG TGTTTGGGAG AATAAAAGAT 120
GAACCTTTTT TTTCTTTGTC AGATCTTGCG CTCATTTGGT TCTGGTGGGG AACAACAGCT 180
ATGAGAGAAC AAGTGTATTC AATTAGAATT AATTCCCCTC TCTTATTCTC ATAGCTGAGC 240
AGGGCTCAAG TGCCTCTCAT CTGAAAGAGG TAATAAGATT TAATCTGTCT CCTCATCTAC 300
CTTCTGCAAG TATACTCAAC AAATTAGCTC TCTGGACTCT TCCAAATGGA GTTTTATGAG 360
GCATTTGCTA AGGTAAACGT TTTAGACTTT GAACACAGTT CAGATTTCAG GGGCAGTACT 420
GAAATATGAA CTGTGTTGCT AACTGCCCTG CCTTTCAACT CAAGACACAA TAACTTTGAA 480
CTAAAATAAT TATATTTTTG TTGTTTTCCA CTCTGTCCCC AAGTCTATAT CACCACCACC 540
GCTAATCCCA CCCCGCAGGA GCTAACTCCT CCTTCCTGTC CCTGCAAGAT CAAAACTCCT 600
CCTGGAAGCC CCGCTAGCTC TGTCTGCTCA CCTTCATGGC AGATATCGCT ATTGTACTTT 660
TATATTCATT TGTATCATAA GTACTTCAAT GTCCACTTCT TCCACGAGCC CCTGAGACCC 720
TGGAGGGTCT GGACCACACC TAGTTTTTCT CACTGTTACA TCTGCCTTGC CAGGCGCATG 780
GTAGGCGCTT AGTAAGTATT TGGTGAACGA ATGGCTTGTT TGGTGACAGT CCAAAGGCTG 840
GAGGACAGAG GGAAAGCTCC CTCCTGTCGG GCCCCAGACG GGTGGCGCTG ATGGAGAGGC 900
GGCTGGGATA AGGCCTCCAG GACCGAAGCG CGCACCCATA AGGCCCCTGC CAAAAAGACC 960
TTCCTGAAGG CGGAGGAACT GCGAGAGTGT CTACTTTGGC CCAAGGCCTG ACTCGACGAT 1020
CCCAGGGACC CTTGCCCTAA CCGGCCCCGC CTCCCGGGCC CCAAACCCGT ACTCGGCCCC 1080
GCCCAAAGCT CCGGCTCCTA GGGCCCGCCC CTGGCCCCGC CTCGGCCGAC CATGGCCTTG 1140
CTCCTGGGCC TGCCTCAAAC CCTCCGCAGG TAACGCCTCC CGAACGTGAG CCACACTCCG 1200
ATTCCCTCCT CAAACCCCTC CCCGTTTCCC ACACCCTGGA CCCCTCGCTC CGTCTCGGCC 1260
CCGCCCCAAG CCCAGCTCCG TCTCGGCCCC TGAGCCCAGC CCCGACCCAC CTCCCAGTCC 1320
CTGGGTTCCT CCCGACACCG GCGCCTCCCT AAGCTCCGCC TCCCAGGGCC CGAGCAGCGC 1380
CTGGCCATAC CCCCATGGCC CGCCTCCTGA 1410
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