| Tag | Content |
|---|
EnhancerAtlas ID | HS121-21336 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr2:25051030-25053570 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP63 | MA0525.2 | chr2:25051764-25051782 | GGCATGTTGTGACATGCA | + | 6.89 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I024827 | chr2 | 25049774 | 25051676 |
|
Enhancer Sequence | CTGGAGGCCA GGACGGCGGG CAGGGACACA CGTTCAAGAG AACAGCAGGT GCTGGTCACA 60
GAGGGCTGTG CATGGTAGTG CACGCTCAGC TGCCACCTCC CGCGGCTCCC CCAGAAATAC 120
CGGGAAAGAT GGGGAAATTT ACCAGGGACT AATCATATGA AAGTTAGTAA CTGCAGCTAA 180
GAGCCTCGCC GTTGCCTCAT TTGACATTCA CAAAAACTCT CTCGAGTATT TTTAGTACTG 240
TCCCTATTGT ACAGAAAACT CGGGCCAGAT TTGCCCAAAC ACAATTAGCA AGCAGAAAAG 300
CCAAAAGTAG GAGCCAAGTC TTTAGGCTTC AAATCCAACA TGTTCTTCCC CATATCACAC 360
TGTTGCTTCA GGAGGGGCCA CGGGACCATG AGCCCCACTC ACAGCCTCCC CGTGATGACA 420
GCTAGTCTCT GCCCAAATCC TTCCATTGGG GGGATGTTCA CTGCCTTCTG GATTCTTTAC 480
TGGTTCTGCT ACTGGGCAGA TGCGGCCGGG AGAAAGCGCA TCCAGAACCG GAATCAACCC 540
CCCCTTTTTG TAACTTTCAC CCACAGGGCA ACCTTGTCTT GCTTGCGCGA TTCCCGCCAT 600
GTCATTCTAG CATGAGCAGT TGTTACACCT CCCTAGCTTT TTACCCCTCC ATGAGTGACA 660
GCATCTCCAG GTGTCCTGTA CAGTGTCCAG GACCCCATGC AGTGGTGACC TCCACACCTG 720
GGTGCCAGGT TCCAGGCATG TTGTGACATG CAGGGGGCCT GGGGCTTCTC TTCCCTGGGT 780
AGTGGGCACC AGCAACCCCT GGCCAAGGTA GGCTCTGGAG CCCCTAACTC CTCATTCCCA 840
GTAGACTTAT TCTTTTTTTT CTTTTTTTTT TTTGAGATGG AGTCTCGCTC TGTCGCCCAG 900
ACTGGCGTGC AGTGGTGCAT TCTTGGCTCA CTGCAACCTC CACCTCCCAG GTTCAAGCGA 960
TTCTCCTGCC TCAGCTGCCC AAGTAGCTGG AATTACAGGC TCGTGCCATT GTGGCTGGCT 1020
AATTTTTGTA TTTTTAGTAG AGACGGGGTT TCACCATCTT GGCCAGGCTG GTCTCAAACT 1080
CCTGACCTCA AGTGATCTGC CTGCCTCAGC CTCCCAAAGT GCTGGAATTA CAAGTGTGAG 1140
CCACCGCGCC CGGCCCCCCA CTGGACTTCT GATTAGCTGC AGCCCTGGAG CTTTTTCACT 1200
TATACCACTG GCAGAATAAG TCTCCATGTT GGTTGTATTT GTGTGCTCCA ATTTTTTTTT 1260
TTTTTTTTTT TTTTTTTTTG AGACAAAGTC TCACTCTGTT GCCAGGCTGG AGTGCAGTGC 1320
ACAATCTCGG CTCACTGCAA GCTCCACCTC CCGGGTTCAC GCCATTCTCC TGCCTCAGCC 1380
TCCTGAGTAG CTGGGACTAC AGGCGCCTGC CACCACGCCC GGCTAATTTT TTTGTATTTT 1440
TAGTAGAGAC GGGGTTTCAA CTGTGTTAGC CAGGATGATT TCGATCTCCT GACCTCGTGA 1500
TCCGCCCGCC TTGGCCTCCC AAAGTGCTGG GATTACAGGC GTGAGCCACT GCGCCCGGCA 1560
CCGTGTGCTC CAATTGTTAA AGTACAACAA TAACATTATA TTTGAAAAAA AAGGAAGATA 1620
GTGTATATGG TACTACCACA ATTAGAGGAG GCCGTGACAA CTGACAAGAG AACACTGATG 1680
ACAGCTCCAG GCATGTAGTG CTCAATACGT GCCCAGTGGT TCTAAACCAA TAGATCTGGG 1740
CTCCCAACTC CTGTCCCTTT TCCCCAAGAA AGCATTTGGC TGCCCCCTCA GGGAGGAAGA 1800
ATACACAGGA CTGGGACTTA GAACTGCCTC CATTCTGGAC TCTGTCACTT CCTGGCTGTG 1860
TGACCTAGAG CAAGTGAATT ACCTTTTTTT TTTTTTTTTG AGACGGAGTC TTGCTGTCGC 1920
CTAGGCTGGA GTGCAGCGGC TCAATCTCGG CTCACTGCAA CCTCCGCCTC CTGGGTTCAA 1980
GCGATTCTCC TGCTTCAGCC TCCCAAGTAG CTGGGATTAC AGGTGTGCAC CACCATGCCT 2040
GGCTAATTTT TGTATTTTTA GTACAGATGG GGTTTCACCA TGTTGGCCAG GCTGGTTTCG 2100
AACTCCTGAC CTCGTGATCC GCCCACCTTG GCCTCCCAAA GTGCTGGGAT TACAGGCGTG 2160
AGCTACCGCG CCCAACCAAT TACCCTTTTT GAGAGTTAGT TTCTCCCTAT GAAACTGCAG 2220
ATACTGGTAC AACTGCTCAG GACTTTTTCA CAGATTAAAT GAATCAACAT ACATAAGGTA 2280
CCTAGCACAG GCCTGGGCAC ATGGAACTGT GCTCTCGGAC TCTGGGAGAG GAGCTTCAAG 2340
GAAACAAGTC CATCCCAGAG GCTCCCTGGA TGACAGGGAC AAGACTCCTT CCACTAGGTG 2400
GGGATGATGT GTTTGGGAAC CTAAGAGCCA CTCCAAAGCT ACATGACGGT GGAGGGATGG 2460
ACTGAGAAAC TGCTTGTGTG ACCCAAACAG AAGCCCTTCT CCACTGAGAA CAGGGGCGTC 2520
CCTTCAACAA GGACAGCAGG 2540
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