| Tag | Content |
|---|
EnhancerAtlas ID | HS121-18805 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr19:3641810-3642900 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr19:3642375-3642393 | GGAAGGACGGCACGCAGG | + | 6.1 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGGCAATGG GAGGTTGTGC CTCGGTTTCC CTCCTCACTT CCCCCATCCT ACCCCCAGGA 60
GTGCCCAGTG AACTCCAGGG CCAGTCCCAG AGGGGAGTTG GGAGCCTCCT GATTGGGTCT 120
GTTCTTTCTG GCTGTCACTC CCAGCCCGGG GACTGTCCAC CTGGGTCCCT TGGTGACTGT 180
GGTGCCAGCA GGGCCTGGGG TGTAGCGGGC TCTGGGGGCA TATGAGCAAA TGGCAGCCCC 240
GACCGGTGTG GGTGCCACAG ACCCTGCCCA CCCTCCAGGC AGTGCCTGCA CCTGGCAGCC 300
GAGGCCCTGA CACAAGTGAC TCAGTGTCCC GGCCGCCGGG CCTGGCCATG TAACATGTCT 360
CTCCAAATGG CACGCTAGAC TGCAGGGAGG GTCACATCCC ACCCAGGGCA CCAAGGGGTT 420
TCTTTCACCA GGCGGCAGCG ATTAAAACAC GGTTAAGAAA AGCAACACCG CGCCACTGCC 480
CCAGTGTTCA CAAGAGTGAG ACCCCAGGGA CCTCGCAAAT GTCCCCGAGG GCTGGGCACT 540
TAAAGCCAGG TGCAGTCCAT GGGATGGAAG GACGGCACGC AGGCGTGACA GGAACGGCGC 600
GCACCCACCC CTGAGATCCC CGTCAGTCGA GTGACAACAG CAAGGTGTGG GCGGCGTGCA 660
CGGGTGTGCC CATTTGTGTC AAAATAAAAG GGAACCACAA GCCTGGTGCA CGTCTGCTGT 720
GTTCCCAGAA AGTATCTTCC AAGAGACAAA ACCCACAGTC CCAGTGGTTG CTCCTGGGGA 780
GGGGACAGGC CGTGGGCAGG AGGGGGCGCA TTTCACGATA TTCCCTCTTG TATCTTGTTT 840
TAAGTTAAAA AAAAAACTTA ATAGAAGAAG AAATAAGGAA GGATCCACAG ACCAGAGCTG 900
CCCTGGCTCT GGCTGTAAGA AAAACAAAGT GGCTGGAAGA TTGTGTGCGG TGCTAGGGCC 960
GAGTGCTACA ATCTTAAATC TGTCCCCAGG AGAGAATGGG CAGAGAGCAG AGGGGCTGGG 1020
GGGCGGGAAA CGGAGCTGGG AGCTGTGCAG GAGGAGCTGG TGAGACCCAG GGAAGGAAGG 1080
GGGTTGGGTC 1090
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