| Tag | Content |
|---|
EnhancerAtlas ID | HS121-05832 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr11:552700-553960 |
Target genes | | Number: 40 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:553482-553500 | GGAGGGAGGGCAGGCAGG | + | 6.44 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGGTACTGAG CCTGCCCGCC TGCCCCCCAG TGCCTGGGAG TGACCAACAC CCCACTTCTA 60
TAGGGGGGCC CTTACCCCAG ATCAGATGTG TCAACCTGGC CCTGCTTCCT CAGCCATGCT 120
CTGAGAGGGA CTGTAACAGG GAGGCCCCCT TCTGGGGGTG GGGGGCTCAC GACCAAGGGA 180
GGCCCAACCC AAGTCCTCTC CCAAGCCACG GTCCAATCCC TGTGACCTTG TGTGCCACCC 240
GGGCTGGACG AAAGAGAGGC GTTCCACAAA AGGGGGTATG AACAGAGTCC AGAGGAGTCG 300
GGACAGAAAG AAGGAGCCAC CCCAGGGCAC CAGCAGGCAG AACATGGCCA CTGGGCAGCT 360
TTCAGGGACA CAGGCATGAG TCCGGGGGCT GGGAGGAAAG GCGGCCAGCA GCCCCACTGG 420
GAGACCAAGG CAGGAGGGTG CTGCCGCTTC ACCCTGAAGA TGGCACGCGC ACTTGGGGAC 480
ATAGAATTAA GCCATGCAGT GCCCTTTACG AAGGACACTG ACTTCAGTGT GATCACAGCT 540
GCAAAGCAGA GAGGACCCTC CCTCAGCGGG CAGGCAGGCC GGGCAGGGGG CAGTGTAAGC 600
AGGGGCGACC CCACGGTGGG CAGCTGACCC TCCTCTGTGC AGGAGCCTGG TTAAGGGGGC 660
TGGGATGGGC AGGGAACAGG GCAGGCCAAG CCTCTGCTCT TCCATATGGT GGTGGGTGTC 720
TGTGGAGGGG GCAGACAGAG GGGTCAACAG CTGGTTACCT AGTGGCCGTG ACCTGCAGGG 780
GTGGAGGGAG GGCAGGCAGG GCGGCCAGGA GGAGGGGAGC TGCAGTGGCC TCAGGGCAGG 840
GTCAGGACAA AGGCATGCCA GGGCTCCAGA CACCGGTGGA GGCGGGTGCT GGGGGACCCA 900
AGGCTTGGGA ACCGGCCCGG GGCGGTCAGC CAGTGAACAG GCTCTCAGGG TCAGGACACA 960
GATGACCGAG GGTCAGAGCC AGGCCTTGTG GTCTCCTTCT CAGGGACAGG ACACAGAGGA 1020
CCCAGGGCCA GAACCAGGCT TCGTGGCCTC CTTGCCTGCC CCAGAGGTGG GCCCGCCCAT 1080
GCGAGTCAGG GGTCACAGGG CTGGGAACAC AGAAAGTGGG GTGCAGGGGT GCTGCTGCCT 1140
GTGGACCCCC AAGGACCACT GCCTCGGGGC TGCAGGGCCA CGGGTGGGCT GTGGCCTCCC 1200
CACCGGGTGA CTCCCTTCCC TGACAGCCTT TCTGACGTCC CATCACTCTG CTTGCTTTCT 1260
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