| Tag | Content |
|---|
EnhancerAtlas ID | HS180-02817 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:117080010-117080550 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DMRT3 | MA0610.1 | chr1:117080478-117080489 | ATTGATACATT | - | 6.62 | | JUN(var.2) | MA0489.1 | chr1:117080338-117080352 | ATGAGTCATTTATT | - | 6.38 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_09788 | chr1:117079120-117088914 | CD14 | | SE_19688 | chr1:117079352-117081415 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_28774 | chr1:117080386-117082718 | Fetal_Intestine_Large | | SE_32513 | chr1:117080479-117089910 | GM12878 | | SE_59077 | chr1:117079459-117152311 | Ly3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 117080047 | 117080432 | | chr1 | 117080073 | 117080476 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I116537 | chr1 | 117078903 | 117082377 |
|
Enhancer Sequence | TTTTAATTCC ATAACACGTC TGACTCAAAG CATTTTGTGA AAGGAAAGTC CATAATACAT 60
CTGACTCAAT ACATTTTGTG AAAGGTGGAG CTACACAGAG CCTTGTCGGG CCCTGCCTAT 120
TGGTTGGGCT GGACCTGTTA ATAGGCAGTG CAGGGAGCAG CATGTGTCAC AGACCTGCCT 180
GTCCAGAGGC CTCACTCCCA CCCTTCTTCT AGGAAGTGCC TCCTATTGGC TAAGGCAGCA 240
TGGACCTACA AGGATGAGTT AAGACACTAA CATGTCACAT TCTGCCATTG TTGCCCTTTA 300
AAAGCCTCAA GGCTAATTAC TTTGTCCTAT GAGTCATTTA TTTGTTAATT CATATGCCTT 360
CTTGCGTCTC AGCTACCCTC CAGCAATTAA TCATAAGAGG CCTGAGGAAA CATGCAAAAA 420
CATATGTAAT ATACAACAAT GGTCATGGTA GCACTGGGAT AATAAAGTAT TGATACATTA 480
TAAACGTCTA CTAAAAAGAG CATTTAAGTA AATTTAGGTT CACCAAGATA ATGGAATACT 540
|
