| Tag | Content |
|---|
EnhancerAtlas ID | HS012-13854 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr16:1807380-1808140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr16:1808098-1808116 | CCTTTGTCCCTTCCTTCC | - | 6.68 | | HNF4G | MA0484.1 | chr16:1808095-1808110 | TGACCTTTGTCCCTT | - | 6.23 | | KLF4 | MA0039.3 | chr16:1807791-1807802 | CCACACCCTGC | + | 6.62 | | Nr2f6 | MA0677.1 | chr16:1808095-1808109 | TGACCTTTGTCCCT | - | 6.19 | | Rxra | MA0512.2 | chr16:1808095-1808109 | TGACCTTTGTCCCT | - | 6.05 | | Zfx | MA0146.2 | chr16:1807934-1807948 | GGCGCCTGGGCCTG | + | 6.41 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I001757 | chr16 | 1807745 | 1808509 |
|
Enhancer Sequence | AGGCGTGAGC CACCACGCCC TGCTCAAGTG ACTTTTTAAT GCCATTTTCC TTTCTGTGTG 60
AAACAACCAA GTAGAAGAGA ACCGCGTCCT CACCTCTGTT GGAGGAAGTG GTGTTTTCCC 120
GCAGAGCGTT TCCCTCGCCA GCCTCCTGTG CAGGGAGGGG CCAGGACCCA GTGAGGATGC 180
CTCGCCCGCC CCACGCTCCC CAGCCCTCCT CTGCTTTCTG GCATGTTCTC TCTGCCCTCC 240
ACAGTGGGGC CCTTGCTCCC ATTGTGACTT CAGTCATCCT TCACCGAGGT CCTGCCCTAC 300
CCAGGCTGAC CCAGAAGCCT AGGAGTCCAG CTCCAGGCCT GCGTCTGCGG TGTCTCCCTC 360
GCCGCTCTCT CCCTCGCCCA CGCTGGGGGG CTTTTGGAGA CTGGGTACCT GCCACACCCT 420
GCCACACACA CTCTCCTCTT CACAGGCCTG CATCATGGGG GCTGCGGGGG GCCTGCCCTC 480
CTGATGGGCG ATGGGAGCAG AGGGCAGCAG GCTTCCGGGT CAGGGCTCGG CAACACAGCC 540
CTGGGCTGGA CCACGGCGCC TGGGCCTGGT TCCCTGCAGG CCTCTGCCTG GGCACACGGG 600
GCACCGGGAC CTGCTGGAGG CTGCTCCCTC TCTCTCCTGC CCTGCAACAT GGGAGCAGCC 660
GAATCATTGC TGGGTTTTCT GTAATAAGAA TGTATTGTTA GTTCCAGTCC CTAATTGACC 720
TTTGTCCCTT CCTTCCCCTG CCTCTCTGTG CGTCGCTGGA 760
|
