| Tag | Content |
|---|
EnhancerAtlas ID | HS012-13838 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr16:789740-790910 |
Target genes | | Number: 39 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr16:790519-790533 | GAGGCCCCGGCCCG | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGAGCAGGAA GAGACCCCAA ATCAGCCCCT GTGAGTGGGC GGAGGTTCCC TGGGAGGCCA 60
GGCCTCAAGG ATGGCTGCCC AGCCGCACAG CCTGAAGGCT CTGCCAGGAG CCATGCACTC 120
AGGGACTGAG GCTGGTCCCA CCGTCTTCTT CCTGCCCCAC TGCTCTCACC CAGGGATCGG 180
GTTCCCAACA TCCTGCGGCA CTGAAGTTCC CAGTGTGCAG GAAGGCCAGT GCTAACAGCG 240
CCTGCAAACT ACCCACCTGC GGAGACACCA CCAACACTGA CCTTCACCCT TCACGTGAAC 300
AGGGGGCGTG ACCACCACAG AGACCAGAGT TGCACTGCCC ATCGAGAGGA CGTGTGCTTG 360
GATCTGTTTG GAGACCACCT CCTGCTCAGT GCCCGGGAAA CAAGTGGATT TCTCTCTCTT 420
CTCCTTGAGA ACCCTGGCAG CCCAGAAAGC CGCCTCCCAG CTCATCCCTG CCGGAAGCGC 480
TCCCAGCAGC CCGCCTCTCG CCCTGCTCAG CTCTGGCCCC GCGGGGCTGT TGGACATGGA 540
CAGGCAGGTG CACCCAGAAA AGGGCGCCTG CAGCCTCCCG GGTTCAAGGG TAGCTGTCCG 600
GCCCACCAGG GCGACGTTAA GGACAGCTCT ACTGAGGAGC CACTGCGGGG CGTCTAGCGG 660
GCCGCCCCTA CTGCCCTCAA ATGAGGTGGG GTCCCCACCG CACCCGTTTA TGCAGATGCA 720
AAGGCTGTGG CTTGGGGGTC CTGAGGCCTG ACAAGGCGTC CTGCGCAGGG GAAGGGGAAG 780
AGGCCCCGGC CCGGGCCCCG CCGCCCTCCA GCTGCGACCC AGGGGTCGGG TTAGGGTTAG 840
GGATGTGTGG GAGCCGCCTC TGCTGCCTCC TCTGGGTTGG GCAGGCCGGC GCGAGCCCGC 900
GACCACGGGA CCCTCCCACG CAGCCCGCCC GGACACCATG GGGCACAGGA GCGGGTTGGG 960
GGGCGCCGCC CTCCCTGGCC TCAGTTTCCT TGTTGGTAAG AAGCGGGCCT CAGTGTCTGA 1020
GGCCCCGCGC CCGGGTCGAT AGAGTCCCTG ACGGCCCAGA CCGGGCTCCC GGGATTCGGA 1080
TCTCATTCCT CAGGGGAGGA AGTGGGGCGC AGAGCAATTT CCCTCCGCGC GACAGGGCAC 1140
CGAGCGCAGC CTCGACCCCG CCCGCCCAGG 1170
|
