| Tag | Content |
|---|
EnhancerAtlas ID | HS050-68545 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr9:36765630-36766520 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF3 | MA0522.2 | chr9:36765870-36765880 | AGCAGGTGTT | - | 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 |
| GH09I036765 | chr9 | 36764998 | 36766650 |
| Enhancer Sequence | AATATTTTTT GAGTAAATAA ACGAATGACT CATGTCGTGC TGGAGGGGGA CTGTGGGACA 60
AGCATCCAGG AGGACTGGAG ATCTCCAGGA GGGACGTCTG AGCAAACAAG AATGTCCCAC 120
ACGTGGAGGT CACTAAGCCC AGGCTGTGTC TGAGATGGTT CTAAGAGAGT AAGAGAGAAT 180
GCACAGAAAG AAACCGGATC ACCTCCTATG CCCCCAGCGC CTGCACAAAG CCTGGCACAC 240
AGCAGGTGTT GCGTGTTGGT TGACTGAATT AATAGATGAA CCTGCTCTTC GGCGAGGAGT 300
GAGACTTCCT GTGCATAAGG GGCTCGAGCA GGAAGACAGC TGGCCGAGAG CGTGCGCTGG 360
GGTCCAGAAG GTTGCCTCAG CTTCACAGGT GCCCATGGGT AACGTGTTGT GGTTCCCCGG 420
AGACTCTGGG CGGGAGGAAG TGGGACCATA GAGAGGGGCC CACTTGGGTA GAGCGTCTAC 480
CTCCGAGAGG TGGAACTTCA TTGGGCGAGT GGGTAGCCAA TGAGGAAGCT CCCTGAGGAA 540
GAGCCCGCCC CTGGAACTGG GCCGAGGCAC CGCCCCCGCG GAGGAAGCCC CGCCTCTCCC 600
CGTCCCTAAC ACTGAGGCCC CAGAGGCGAA CTGTCGGGAC TCCCGGGCTG CTTGGTGGCC 660
TGAGAGGCCC CCGAAGGGCT CTGGGCTGCG CCTTCATCCG CTGCTTTCCT GTGTGACAAC 720
CCCAGACCTC ATCCTTCAGG GGGTCTCCAT TGCCTCAGGT TCCTCTTTTT TTCGAGACGG 780
AGTTTCAGTG TTGACTCCCA GGCTGGAGTG CAGTGGCGTG ATCTCGGCTC ACTGCAACCT 840
CCACCTCCCG GGTTCAAGCG ACTCTCCTGC CTCAGCCTCC CGAGTAGCTG 890
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