| Tag | Content |
|---|
EnhancerAtlas ID | HS080-36818 | Organism | Homo sapiens | Tissue/cell | H9 | Coordinate | chr9:36765210-36766440 | 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 | ACAGGAATGA GACAAGAGGA AGGGAGGGAA GAGACGAGGT GGGGAGGACG GGAAGGCGTG 60
CAGGGAGTGG GCCGGTGCGA GAGGGACATG GGATGGAGTC CACAGGGGAA GAGCTGGGGA 120
CTCCAGGTTT TCTGGTCAGG AGAGACTGGA GACGCCACTG ACAGAAAGAG GAGGAACAGG 180
TGTGGGGAGA ACTGATGTTT CTTCGACCAG AGCCATCTGC GGAAACATCG TCTCCTCCGT 240
GGGGCCCAGC TTTCATTCCT CACAGCAGTG ATCACTGCAT GGCAAACAAT CACATTCATC 300
TATTATTTGT TTCTTGTCTT TGCTCAATCA GCATATAAGA GAGTACGAAT TCCATCTGCC 360
GTGTTCACAG CGCCATCCCC AGAACCTACA ACAGTGTCGG CTTCTAGTAG GTGATCGCTA 420
AATATTTTTT GAGTAAATAA ACGAATGACT CATGTCGTGC TGGAGGGGGA CTGTGGGACA 480
AGCATCCAGG AGGACTGGAG ATCTCCAGGA GGGACGTCTG AGCAAACAAG AATGTCCCAC 540
ACGTGGAGGT CACTAAGCCC AGGCTGTGTC TGAGATGGTT CTAAGAGAGT AAGAGAGAAT 600
GCACAGAAAG AAACCGGATC ACCTCCTATG CCCCCAGCGC CTGCACAAAG CCTGGCACAC 660
AGCAGGTGTT GCGTGTTGGT TGACTGAATT AATAGATGAA CCTGCTCTTC GGCGAGGAGT 720
GAGACTTCCT GTGCATAAGG GGCTCGAGCA GGAAGACAGC TGGCCGAGAG CGTGCGCTGG 780
GGTCCAGAAG GTTGCCTCAG CTTCACAGGT GCCCATGGGT AACGTGTTGT GGTTCCCCGG 840
AGACTCTGGG CGGGAGGAAG TGGGACCATA GAGAGGGGCC CACTTGGGTA GAGCGTCTAC 900
CTCCGAGAGG TGGAACTTCA TTGGGCGAGT GGGTAGCCAA TGAGGAAGCT CCCTGAGGAA 960
GAGCCCGCCC CTGGAACTGG GCCGAGGCAC CGCCCCCGCG GAGGAAGCCC CGCCTCTCCC 1020
CGTCCCTAAC ACTGAGGCCC CAGAGGCGAA CTGTCGGGAC TCCCGGGCTG CTTGGTGGCC 1080
TGAGAGGCCC CCGAAGGGCT CTGGGCTGCG CCTTCATCCG CTGCTTTCCT GTGTGACAAC 1140
CCCAGACCTC ATCCTTCAGG GGGTCTCCAT TGCCTCAGGT TCCTCTTTTT TTCGAGACGG 1200
AGTTTCAGTG TTGACTCCCA GGCTGGAGTG 1230
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