| Tag | Content |
|---|
EnhancerAtlas ID | HS190-12894 | Organism | Homo sapiens | Tissue/cell | Treg_cell | Coordinate | chr9:36765490-36766600 | 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 | GGCAAACAAT CACATTCATC TATTATTTGT TTCTTGTCTT TGCTCAATCA GCATATAAGA 60
GAGTACGAAT TCCATCTGCC GTGTTCACAG CGCCATCCCC AGAACCTACA ACAGTGTCGG 120
CTTCTAGTAG GTGATCGCTA AATATTTTTT GAGTAAATAA ACGAATGACT CATGTCGTGC 180
TGGAGGGGGA CTGTGGGACA AGCATCCAGG AGGACTGGAG ATCTCCAGGA GGGACGTCTG 240
AGCAAACAAG AATGTCCCAC ACGTGGAGGT CACTAAGCCC AGGCTGTGTC TGAGATGGTT 300
CTAAGAGAGT AAGAGAGAAT GCACAGAAAG AAACCGGATC ACCTCCTATG CCCCCAGCGC 360
CTGCACAAAG CCTGGCACAC AGCAGGTGTT GCGTGTTGGT TGACTGAATT AATAGATGAA 420
CCTGCTCTTC GGCGAGGAGT GAGACTTCCT GTGCATAAGG GGCTCGAGCA GGAAGACAGC 480
TGGCCGAGAG CGTGCGCTGG GGTCCAGAAG GTTGCCTCAG CTTCACAGGT GCCCATGGGT 540
AACGTGTTGT GGTTCCCCGG AGACTCTGGG CGGGAGGAAG TGGGACCATA GAGAGGGGCC 600
CACTTGGGTA GAGCGTCTAC CTCCGAGAGG TGGAACTTCA TTGGGCGAGT GGGTAGCCAA 660
TGAGGAAGCT CCCTGAGGAA GAGCCCGCCC CTGGAACTGG GCCGAGGCAC CGCCCCCGCG 720
GAGGAAGCCC CGCCTCTCCC CGTCCCTAAC ACTGAGGCCC CAGAGGCGAA CTGTCGGGAC 780
TCCCGGGCTG CTTGGTGGCC TGAGAGGCCC CCGAAGGGCT CTGGGCTGCG CCTTCATCCG 840
CTGCTTTCCT GTGTGACAAC CCCAGACCTC ATCCTTCAGG GGGTCTCCAT TGCCTCAGGT 900
TCCTCTTTTT TTCGAGACGG AGTTTCAGTG TTGACTCCCA GGCTGGAGTG CAGTGGCGTG 960
ATCTCGGCTC ACTGCAACCT CCACCTCCCG GGTTCAAGCG ACTCTCCTGC CTCAGCCTCC 1020
CGAGTAGCTG GGATTACAGG CGCCCGCCAC CACGCCCAGC TAATTTTTGC ATTTTTAGTA 1080
GAGACGGGTT TCACCATGTT GGCCAGGCTG 1110
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