| Tag | Content |
|---|
EnhancerAtlas ID | HS073-14322 | Organism | Homo sapiens | Tissue/cell | GM19238 | Coordinate | chr9:36765430-36766670 | 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 | GGAAACATCG TCTCCTCCGT GGGGCCCAGC TTTCATTCCT CACAGCAGTG ATCACTGCAT 60
GGCAAACAAT CACATTCATC TATTATTTGT TTCTTGTCTT TGCTCAATCA GCATATAAGA 120
GAGTACGAAT TCCATCTGCC GTGTTCACAG CGCCATCCCC AGAACCTACA ACAGTGTCGG 180
CTTCTAGTAG GTGATCGCTA AATATTTTTT GAGTAAATAA ACGAATGACT CATGTCGTGC 240
TGGAGGGGGA CTGTGGGACA AGCATCCAGG AGGACTGGAG ATCTCCAGGA GGGACGTCTG 300
AGCAAACAAG AATGTCCCAC ACGTGGAGGT CACTAAGCCC AGGCTGTGTC TGAGATGGTT 360
CTAAGAGAGT AAGAGAGAAT GCACAGAAAG AAACCGGATC ACCTCCTATG CCCCCAGCGC 420
CTGCACAAAG CCTGGCACAC AGCAGGTGTT GCGTGTTGGT TGACTGAATT AATAGATGAA 480
CCTGCTCTTC GGCGAGGAGT GAGACTTCCT GTGCATAAGG GGCTCGAGCA GGAAGACAGC 540
TGGCCGAGAG CGTGCGCTGG GGTCCAGAAG GTTGCCTCAG CTTCACAGGT GCCCATGGGT 600
AACGTGTTGT GGTTCCCCGG AGACTCTGGG CGGGAGGAAG TGGGACCATA GAGAGGGGCC 660
CACTTGGGTA GAGCGTCTAC CTCCGAGAGG TGGAACTTCA TTGGGCGAGT GGGTAGCCAA 720
TGAGGAAGCT CCCTGAGGAA GAGCCCGCCC CTGGAACTGG GCCGAGGCAC CGCCCCCGCG 780
GAGGAAGCCC CGCCTCTCCC CGTCCCTAAC ACTGAGGCCC CAGAGGCGAA CTGTCGGGAC 840
TCCCGGGCTG CTTGGTGGCC TGAGAGGCCC CCGAAGGGCT CTGGGCTGCG CCTTCATCCG 900
CTGCTTTCCT GTGTGACAAC CCCAGACCTC ATCCTTCAGG GGGTCTCCAT TGCCTCAGGT 960
TCCTCTTTTT TTCGAGACGG AGTTTCAGTG TTGACTCCCA GGCTGGAGTG CAGTGGCGTG 1020
ATCTCGGCTC ACTGCAACCT CCACCTCCCG GGTTCAAGCG ACTCTCCTGC CTCAGCCTCC 1080
CGAGTAGCTG GGATTACAGG CGCCCGCCAC CACGCCCAGC TAATTTTTGC ATTTTTAGTA 1140
GAGACGGGTT TCACCATGTT GGCCAGGCTG GTCTCGAACT CCTGACCTCA GGTGATCCAC 1200
CCGTCTGGGT CTCCCAAAGT GCTGGCATGA GCCACCGCGC 1240
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