| Tag | Content |
|---|
EnhancerAtlas ID | HS050-46895 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr3:47653150-47654060 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr3:47653769-47653785 | ATTCTTTCTAGGAATT | + | 6.73 | | BCL6B | MA0731.1 | chr3:47653770-47653787 | TTCTTTCTAGGAATTTA | + | 7.13 | | Foxo1 | MA0480.1 | chr3:47653623-47653634 | TGTAAACAGCA | - | 6.14 | | HSF1 | MA0486.2 | chr3:47653637-47653650 | GAATCTTCTGGAA | - | 6.06 | | STAT1 | MA0137.3 | chr3:47653541-47653552 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr3:47653541-47653552 | TTTCTGGGAAA | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCAAAAACTA GATGGAATAA GCATGAGAAT TAGCCTAAAA ATCTGGGCCT TTGGCAGAGG 60
GCCGACTGGG GAAAATCCCT GTGAAATTGA GTGAGAAGCA TCACTGGTTA TAGGAGTAGC 120
AACTGGGGTA TTTCCATGGA CAGATGGGGT GTGGGAAGAC AGGCCATGAA CACAGTATGA 180
AGAAAAGATG CATGAGCAGG CTAAGAGGAG AACAAATAAA GAGAGTAAAC GGTATAGCTT 240
ATGTCCTGGA TTTTGGTAAC TGGCTTGTAG ACTTTCCTTA GGGAGAGGGA GATTTTCTGA 300
AACAAAACAT TTTGAGAGAG GTTGAGGGTT ACCAGGAACA AGCAAGACAG GGTTCTACCA 360
TGGTCCTAAT AGTCTAGTGT GGGCTCTTCA TTTTCTGGGA AAGGTAATCT GAAGAGGGTA 420
AAGCCTAGCC TGGTTCAGTT TCCTGTGTGC ATGATGAGAA GGGAGATGTA ATATGTAAAC 480
AGCAAGAGAA TCTTCTGGAA GTCCAGTTCT GCAGGAAGAC TAATCAGATT AGTAAGTAAG 540
AGGCAAAATG ACTGTAAAAG GTGGGGTGGG AAATCTAAAT ATTCTGGCTA CAGATCCTTG 600
GTTTTGCTTT CTTCTAATCA TTCTTTCTAG GAATTTAGGA CTCTGAATTT GCTTAAGAGG 660
TGGCCAGAAA ACATCCTCTT ATCTGTTTTT GTTGAGTGAC TACTGGTCTG AACAGCTTGG 720
CTGTAGTCCT ACTGTTATGT AAGAACTATG GAATTTAGGT CAAGATATGC TTTATAAGGA 780
AGCTGAACTG CTACTGGAGG GAGCAGTGAC TCTAAAAGGA AATTCTGGTC TCTGCATTAC 840
CTAGCTGAAT TTTGGGTTCT GCTTTTAACC AAACTAGCCT TTCTTTGAGG GCTTACCTTA 900
GTATCAAGGT 910
|
