| Tag | Content |
|---|
EnhancerAtlas ID | HS012-25831 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr8:144798610-144799860 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr8:144799525-144799545 | GGATTGGGGGTGGATGGGGT | - | 6.28 | | RREB1 | MA0073.1 | chr8:144799100-144799120 | TGTGCGTGGGTGTGTGGGGG | - | 6.97 | | ZNF263 | MA0528.1 | chr8:144799677-144799698 | TCCCTCTACCTCCCCTCCTCT | - | 6.2 | | ZNF263 | MA0528.1 | chr8:144799669-144799690 | CCCTCCCTTCCCTCTACCTCC | - | 6.42 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 144799188 | 144799437 | | chr8 | 144799014 | 144799600 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I143717 | chr8 | 144799188 | 144799437 |
|
Enhancer Sequence | GGGGTGAGTG CCTGGGGGTG CGTCCGCGCG CCGAGGGGCG CGGCAGATCT GCGGAGAGAG 60
GACCTGCGGG GCGCGGCCGG TCCCCTCGGA GGCCTGTTCC GTCACACACT GGCGTCCTGC 120
CTCCTCCGTA GGCGGGAGAG GTGGTCTGGA GCCCCTTCGT GCCTCAGTTT CCTCATGGGG 180
TAACACGATC CTGACTCCCA GGAACCTGGC TCCTGGAGGC AGGTGACAGC CAGGGCCGCC 240
AGAGGCCTCA GGCAGAGGGA TCCTGGCGCC CCACTCCCCA CGCGTCCACA GTCGCCCGCT 300
TCCCGGGTGC ACACGACGCT CTGGGGAGGC TGGGCCCGCG CCCGGGTCAC TGAGAGGAAG 360
GGCGGACCCC AGGCTCAGGA GCACAGGGGC GAGGCCCGAG AAGGGCCTGA GCGGTTATGG 420
GGTGGGCGCA GAGTGAAGGG CAGAGCCTTG TGTATCTGTG TGTGTGTGTG AGCATGTAAG 480
CCTGTGTGTG TGTGCGTGGG TGTGTGGGGG GGTGTTCGAG GGTGCCATGG GGGAGGGGAG 540
GAAGAGCCTT CCAGGCAGTG CAGACGGTAA GTGCGTAGGC CCAGTGCAGG GTTGTGTATG 600
TGCAACTGGA TAGGAGATGG AGAGAGACAG GTGAGTGGTG AGGGTCCGAT CGTGTGGGAG 660
CTTTGGGGAA CTTCCAAGAC TTTGGTTTTT ACTGTTGCTG AGGCTGGGAG CTGTAGCAGC 720
TGCTGGTGTC ACTTTACAAG GCCCACCCCT GTGCTGAGGA CCTACCGTGG GTGTGCACGG 780
GAGCGGCAGA CGGAGATGAG TTAAGGGGTT AGCGTAGCCA CGCAGCGAGA GATGCCAGAG 840
GCTGGGACCA GGGTGGGGGC AGAAGAGACC GTGGCAGGGG CTAGATTCTG GAGGAATCTG 900
AAGGTAGGGC CAATGGGATT GGGGGTGGAT GGGGTGTGAG AGAAAGGGAG GGAGAGTGCC 960
TGGGCAGCTG GAAGGATGAT AGGGCATCCC CGAGCTTCAT TTCCTGCCCA GACGCTCCCC 1020
TCTGTGGCCT CCTTTCCTCC AGGGCCTCGC CAGCTCTCAC CCTCCCTTCC CTCTACCTCC 1080
CCTCCTCTGG AAGATGTCGG AGTCTAGGGC AGCCTGCAGT TGCGGGAGCC CACACTCCCA 1140
TCCCCTCTCG GGACCCAGGA TGGGAAGGAG GAGCCTCATG TCTGTAGGGA CAATCTGGGT 1200
GGGCAGGGGA TGGGGGGAAG GGGCTGGCCC TGTGTGACGG CACTCCTTCC 1250
|
