| Tag | Content |
|---|
EnhancerAtlas ID | HS101-05562 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr10:79702540-79703640 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr10:79703562-79703575 | ATGACATCATCAT | - | 7.52 | | JUND(var.2) | MA0492.1 | chr10:79703561-79703576 | CATGACATCATCATT | - | 7.2 | | Myod1 | MA0499.1 | chr10:79702934-79702947 | AGCAGCTGTCTCC | + | 6.21 | | Myog | MA0500.1 | chr10:79702933-79702944 | CAGCAGCTGTC | - | 6.14 | | Tcf12 | MA0521.1 | chr10:79702933-79702944 | CAGCAGCTGTC | - | 6.02 |
|
| | 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 |
| GH10I077941 | chr10 | 79701561 | 79704826 |
|
Enhancer Sequence | TGTTGGCCAG GCTGGTCTGG AACTCCTGAC CTCGTGATCT GCTTGCCTCG GCCTCCCAAA 60
GTGCTGGGAT TACAGGCATG AGCCACTGCG CCCGGCCATA ATTTTTGTGT TTTTAGTAGA 120
GACAGGGTTT CACCATGTTG GCCAGGCTGG TCTTGAACTC CTGATGTCAG GTGATCCACC 180
CACCTTGGCC TCCCAAGGTG CTGGGATTAT AGGCGTCAGC CACCGCTCCC GGCAAAACCT 240
GAATTTTTAA CTAGCATGCT GGGTGAATTT TATCAGGACA GTGAACCAGG ACTCTCTGAA 300
ATCCCTTCCC CGGGATAGTC AACGAGGCTT TCAATTTAAA CTTGCATTTG AAGCTTGCAG 360
AGACTCACAC TGACTTACCC AGGCCCTAAC ACACAGCAGC TGTCTCCATG GTTGCGCCAG 420
GTAGTGAAGG ATACAGGGCA GCAGGAAACG AGTCCCGGTT CTCAGGTGGA TCCCGTGCTT 480
CCACCTCTGT TAGAGCCCAG GCCCTGAGGG CATAGGGCCA AATTGCCACA GAGCTCCAGA 540
GAAATCTGTC TCTCCCGTCC CCCACCCTAA GACTGAGCTG CTGGAGGAAA GAGGCCAGGT 600
TTGTTTCCTT TTATTGGTTA ACTCTCTTCA GTCGCCCCTT TCTCCTGCAG ACACCTTGGG 660
GACTTTTAGT AATTGTCAGC TGAATGAATA AATTAATGAC AGAGGGAGAC AGACGTGTTA 720
ACAGCTAACA GTAATTCAAG CAGAATGGAG TAAGTGCTAA ATAGTGGTGG AATGAGTCAT 780
GAATGCTGAC AGGGAAGGAA GAGGGAAAAA GGCATTCATT CTCTCCCCCT CCACTGTCAA 840
AACAGTGCCT TCACTCTTCC TCCCTCCATC TCTCTTACAG GCACCAGAGA GCAGAAAATG 900
TATGTGTATA GTTTCAAGAA CAGTTCCAAA GCAAACACCC ATATAGTCAC CCCCATGTGC 960
TGGCCCCCAG GATAAGAAAT AGAACCTTGC CAGAACCTCA GAAGCCTTTC CTGGCCCCCT 1020
CCATGACATC ATCATTCCCC GCCTCTTGCC CTCATCTAAC TTCTAATCTG ATTCTGAGGG 1080
GAATCATTTT CTTACTTTTC 1100
|
