Tag | Content |
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EnhancerAtlas ID | HS121-07326 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr11:71193070-71193890 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr11:71193835-71193846 | TATGTAAACAT | + | 6.32 | Foxa2 | MA0047.2 | chr11:71193833-71193845 | ACTATGTAAACA | - | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 71193191 | 71193275 | chr11 | 71193349 | 71193409 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I071479 | chr11 | 71190725 | 71193783 |
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Enhancer Sequence | AGTAGGTGAC ATCTGTTGGC TTGAGGGAGG CTCCAGGGTC CAGCCCTTGG GCTGCCTGAG 60 TTAGGGACCT AGGAGGGGGC AGAGGAAACA CCCGTGCCAT GGACATCGGG GTGAAGGGGG 120 CTTTGTGGCC ACGCACAAAT GTCACAGCAT CACATCCCAG TCCTGCAGCT AAGGCAGCAA 180 GGCCATCAGT AGCTTCCTGG GGCTTCGGGC CCATGTGGCT GAGTCTCCAG AGCTGTACCT 240 GCCTGCTCTG TGCACGGTGT GGCCTGGTGG GGAGAACACA GGCGTCGGAG GTTCACATCC 300 TCCCCCATGT GATATAGTAT CAGACATCAC CTTAGCATAT GCAGCAGAAC AGCGGTGATG 360 ATGCCCGATG GATGGGGCTG TGGGCCATAG CCTGGGCTGG CGCTGCACAG GCACCTGGGG 420 GTGTAGACCG GGGTGCAGCC GTACGGGCAC CTGAGGGCTG TAGACCGGGG TGCAGCCGCA 480 CAGGCACCTG GGGGTGTAGA CCGGGGTGGA GCCGCATGGG CGCCTGGGGG CCGTAGACTG 540 GGGTGCAGCT GCATGGGCAC CTGGGGGTGT AGACCGGGGT GGAGTCACAC GGGCACCTGG 600 GGGTGTAGAC CGGGGTGGAG CCGCACAGGC ACCTGGGGGT GTAGACTGGG GTGGAGCCGC 660 ACAGGCACCT GGGGGTGTAG ACCGGGGTGG AGCCGCACAG GCACCTGGGG GTGTAGACCG 720 GGGTGGAGCC GCATGGGCAC CTGGGGGTGT AGACCGGGGT GGAACTATGT AAACATCCCA 780 CACACTCAGG TGACTTCCAC CCATTCTGTC CTGGTGGTTT 820
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