| Tag | Content |
|---|
EnhancerAtlas ID | HS050-39388 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:191624300-191625300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr2:191624567-191624578 | GGATGACTCAT | + | 6.62 | | JUNB | MA0490.1 | chr2:191624567-191624578 | GGATGACTCAT | + | 6.62 |
|
| | 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 |
| GH02I190759 | chr2 | 191624240 | 191625242 |
|
Enhancer Sequence | TTGTTTTTAT TTTTATTTTT ATTTTTTTTT AAGGCCAAAC ACAAATCCAT CACAATTCTG 60
GCACTTACTT TAAATGATAG GGTATTGGGC CGTATTTGTC AATCTCTTGT AAAGAAACCA 120
GGGTGTTTTT ATATTTACCT GAATATGTCT TTCTACCTCC ACCACCTTTT CCATATTCAT 180
TCATGTAAAT TATAAAAGTA AGGCAGTTAC TGAGCCCAAT ATTCACTGAT AACAAAGCAG 240
GAAGCTTATG GGTATGAATC AGAGTGTGGA TGACTCATTA AAAGCCAAAT GTTTGTACGG 300
AAAGCTCCCC TAAAATGGCA CAAAAGCAAA TATTTATAAA CATGTTAAGA AAGCATTGTG 360
GAACTCTTGG GAGGAGGGGT TAAAATATTG CCACACATTC CTAATTACAC TATTACAATA 420
AAACATTGCT TTGCTACCAT GAAGTCTGAC CCAGGCTCTA AACTCTTTAG CAATGGGGTT 480
GCTCTAATTA GCTATAATAA GACTGATCCT GACTCACAGT GTGTCCGGAA TTGGTGGGTT 540
CTTGGTCTCA CTGACTTCAA GAATGAAGCC ACGGATCCTC GCGGTGAGTG TTACAGTTGG 600
CGCGTCTGGA GTTTGTTCCT TCTGGTGTTC GGATGTGTTC GGAGTTTCTT TCTTCTGGTG 660
GGTTCGTGGT CTCGCTGGCT CAGGAGTGAA GCTGCAGACC TTCGCGGTGA GTGTTACAGC 720
TCTTAAGGCG GTGCGTCTGG AGTTGTTCGT TCCTCCCGGT GGGCTGGTGG CCTCGCTGGC 780
TTCAGGATTG AAGCTGCAGA CCTTCCCGGT GAGTGTTACA GCTCATAAAA GCAGTGTGGA 840
CTCAAAGAGT GAGCAGTAGC AAGATTTACC ACAAAGAGCG AAAGAACAAA TCTCCCACAA 900
CATGGAAACG GACGCAAGCT GGTTGCCACT ACTAGCTCAG GCAGCCTGGT TTTATTCTCT 960
TATCTGGCCC CACCCACTTC CTGCTGATTG GTAGAGCCCA 1000
|
