| Tag | Content |
|---|
EnhancerAtlas ID | HS158-14814 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr12:132533650-132534860 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr12:132533722-132533732 | GGGGCGGGGC | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAGTGGTCGG ATGTGTGCGT GAGTGGGACA GCCCCACCTC TCAAAGCCTG CGGGGGCTCC 60
AGCAAGCCAT GCGGGGCGGG GCATTCATGC CTGGTTAGAG CCTGCACAGG AGTTCCATTA 120
CCAGACACAC GGTCTTTCCA TCTCTGACTT GGCTCAGTTG AGCCATCCAG TGTCATGTGT 180
GATAGGCCTG GTATTAGTCT TATGCACCCC TTCTCCCTGC TTCCCTTTGC TTACTCTTAG 240
GATAATAGGT AGGAGGAGAA TGCTTCCCTG TATGGTACAG TGTTCCGGAA GCAGACTGCT 300
GTGGCCTTGC ATGTTGGTTT CTAGTTCTGG TTGTCCTTGG TGTTGCCTTC AGAATTTAAG 360
GCATTCCTCT AGCAGTGGAG GACACATGTG CACACAGACA TGTATACATG TACCTGCACA 420
GACACACCCA TACCTGGGCC TGTGCTGCTG TGTCATGTGA GAGTCTTGGT TTTCGCCTTG 480
GCACACTCTC TTTGACCAGG GTTTAGAGGA GCATGGGGGA AGAGCCCTGG GTGAGGAAGG 540
AGGTGCTTGA GCCCTGGTCT TGACTTGTCG CTACCTCTGT GACCTTGCAC AGACAGCATT 600
CCTGGGACAG CTGTTCACTT CACAGGATAA GGAGTTGCTT TAAAATTCTG CAGGATTCTA 660
AGATGTCTTG GGAGCACATA GCCCACAATT GAGTGGCCCA TTGTTTAGCT GTGCCATTTA 720
TGAAGGAAAG ACTGCCAGCC ATAAGCACTG CTAGAGACCC CAAGAATGTA CTTTGAGACA 780
CCACTGGGCA TGCGCCAGCC TCACTGTCCA CCGTGGGCAG ATGACAGTGT TGTCCGTGGC 840
AGTCCGCGCT GCCCCTTGGT GTTAGCGGGT GAAGGCTCAC AGCCCGCTCC ACACAGTCAC 900
CTGCCATGTG ACCTTGGGCA CTTTGCACAC CTGTTTTGTT CCCTCTCCCT CTTGGGGTGA 960
TTATGGGGCT TACGTGAGAG AACACCTGGA AAGGATTAGC ATGGACTGGA GAGTGTCACA 1020
GCAGTCGGCC GCGACAGCCA CTTAATGCCG CTGCTGTTGG GTTATGCCTG AACTTGGAAA 1080
GAAGGCCCAG GAAAAGGAAG TTTGTGTTCA GCCATGGGGA GTTTAGCCTC AGATTCCCAC 1140
CCAGTGAGCC CTGTGTCCCA CGCAGCCGTC TGTCCATGCT GCCTAATTCA GATGCACTCT 1200
CGTCAATTTC 1210
|
