Tag | Content |
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EnhancerAtlas ID | HS120-01258 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr11:74392700-74393340 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr11:74392975-74392987 | GCTATTTTTAGA | - | 6.52 | MEF2B | MA0660.1 | chr11:74392975-74392987 | GCTATTTTTAGA | - | 6.22 | MEF2C | MA0497.1 | chr11:74392974-74392989 | AGCTATTTTTAGAAG | - | 6.52 | ZNF263 | MA0528.1 | chr11:74393078-74393099 | CCTCCCGCCTTGTTCTCCTCC | - | 6.1 | ZNF263 | MA0528.1 | chr11:74392765-74392786 | TCCTCCCTCTCCCCCTCATCA | - | 6.82 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_55068 | chr11:74392021-74394979 | Stomach_Smooth_Muscle |
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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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Enhancer Sequence | TGTGGGCAGT GCTGTCTCCT CAATCCACCT TATCGCCAAG ACTGTCTTCC TCCTGACATC 60 GCACATCCTC CCTCTCCCCC TCATCAGTTT GGGACAAGCC CCATCTTCAC GAGGGTCTCT 120 CCCCTGGATC CCACCTAAGG CTGTGGCTGC CCCGTCCCCT GGGGGAAGAG GGCAGAGTGA 180 CATGTCTGCT GACAGACTGA TGGCCCATGC TCCAAGGGGA GCAGGCCAGC AGCCGCAAAG 240 GTGCAGTCTG TGCCAGGTGG GCCTTGCCAG CCAGAGCTAT TTTTAGAAGC CATGTTTGCA 300 GAGTTTGTGT TAATAGTGTC TCTGTCCAAG CTCTGGCTCC CAGGTCTTAG GGAGGGGGAG 360 AGCCTTAGAG AAATCCTCCC TCCCGCCTTG TTCTCCTCCT CACAGGTGGC TGGGATCAGT 420 GGGGGACTCC TATCCAGGTC GAAGCCCTCC CAGCCAGCCA TCTGCAGACA CAGGGCAAAT 480 AGGGGCTGGG GGGCTAGCTC GAGGGAGGAA GAGAGGCACA GAGCTGAGGC TACCAGAGAA 540 CCAGTCTCAG AAGGGAGGCA GGACCCCCAG CCACAGGACA CTCCATCGGT GCCATGTCAC 600 TGGATGGACA CTGTCAGCCG CCTTATCAGT CACCTCCTTA 640
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