Tag | Content |
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EnhancerAtlas ID | HS182-21892 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr9:116728500-116729580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr9:116729051-116729062 | CCACACCCTGC | + | 6.62 | Nr5a2 | MA0505.1 | chr9:116728603-116728618 | CCAGGCCTTGAACTC | - | 6.06 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I113964 | chr9 | 116726436 | 116730118 |
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Enhancer Sequence | GTAGGTCCTG TGATGAGCAT CTTGCCATTT TGCAGAGGGA GAAATCGAGG CCTTGGAAAT 60 ACGTGTGACT TGCTGAAGAT CGCAGAGCTA GAAAACGGCA AAACCAGGCC TTGAACTCCG 120 ATGTTCTAAC TCTAAACTCT GTTCTCTTAA GCTTCGGTTC AAATTGAGAC TCAGGTCAGT 180 TTGCACAGGG TACAGATGAG TTTGCTGTTT AGGTTGAATC ATATGAAACT GCTGGTGTTA 240 GAACATTTTG GCCTCAGCAC ATGGCAATGT CAGAGGTTCA GCTTAATCCA CTTGGAAGGA 300 ATGGCTGTGA TGTATTTGTA AGGACAGACC ACACCGGCCT GGCGTGTATG GAACTCCACC 360 CTGGGAGTTG GTGTTCCCAA CACAGTGGAC TTTGGCTCTG TCGTCATGGT GTAGCTGGAC 420 TCGGCCAGGC CCACACGCTG TGATTGCCAG GTGCTGTGAT ACTGACACAT GTGTCTTGGA 480 CATCTCCCAC TGAATCCATT GTCCATCCAT ATTCCAATGA AGCAACTCTC ATCTGCCACC 540 ATCTGAACAT CCCACACCCT GCCCAGGTAG AACTCTCCTC TAGTTGCCCC AGTTTCCCAG 600 CAGCACCACC TGAGTCTCTG CAAAAGTATT TGACAATTCT TTGAATATTT TTAGCACTTT 660 CTCTTTGTTT TATGAAAATG GGTGGAAAAC AGAAATGCAT GCAGCTACCA GTAACACGAA 720 GCTGAAGTAT CATTCACTCA ATAAAAGAGA AACAAAGGTG GAGATTATTA GGCATGCTGA 780 AAACAGAGAC TCTTATCCCA CACTCTGTCA CGTGTTTGCT GCACTTGAGC TGGTCAACTC 840 TGTGTGAAAT TGTGAAGGAA AAGGACAAAA ATGACAACTT TAAAAGTGTG TGTGACAAGC 900 TAAAAATACA CGCACAGAAT TAAGTCTGAA AGGCGAGAGA TCCATTTGGG AGTTAACCAT 960 TTTTTTAAGA TCTCTGGGGC AGAATTTCCA CCCGTACCAC TTCTGCTGCT TATGATACAA 1020 ACATTCAAAC AAATTCAGCC TGTTTGCTTT GCATACAAGT TTTGAGGAAT GCAAGATGTT 1080
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