| Tag | Content |
|---|
EnhancerAtlas ID | HS121-08611 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr12:50149540-50152000 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr12:50151042-50151057 | TGTCCAAAAATAGCC | + | 6.29 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACGTTAAGGG ATTTGTCTAA TTTTGAGGGG TGAGCTATAT TTTCAGTATC TCTTAATTAG 60
TTCCCCCCCC TTTTTTTTTC TTTTTTTTTT TTTTGAGACA GAGTCTCGCT CTGTTGCCCA 120
GGCCAGAGTG CAGTGGCTTG ATCTTGGCTC ACTGCAAGCT CCGCCTCCCA GGTTCACACC 180
ATTCTTCTGC TTTAGCCTCC CGTGTAGGTG GGACCACAGG CACCTGCCAC CACACCCGGC 240
TAATATTTTG CATTTTTAGT AGAGACGGGG TTTCATCGTG TTAGCCAGGA TGGTCTTGAT 300
CTCCTGACCT CATGATCCGC CCGTCTCGGC CTCCTAAAAT GCTAGGATTA CAGGCATGAG 360
CCACCGTGCC TGGCCCTTTT TTTCCTTTTT TTTTGAGACA GTGTCTCCGT CTGTCACCCA 420
GGCTAGAGAG TGCAGTGGCG TGATCTTGGC TCACTGCAAA CTCTGCCTTC CGGGTTCAAG 480
CGATTCTCCT GCCTCAGCCT CCCAAATAGC TGGGATTACA GGCATGTGCC ACCATGCCCG 540
GCTAATTTTT GTATTTTTAG TAGAGATGGG GTTTTACCAT GTTGGCCAGG ATGGTGTTGA 600
TCTCTTGACC TAGTGATCCA CCCACCTTAG CCTCCCAAAG TGTTAGGATG ACAGGCGTGA 660
GCCATAGTAC CCTGCCTCCT GGCTTTTTTT TTTTTTTTTT TTTTTAAGAT GGAGTCTCAC 720
CCTGTGGCCA GGCTGGAGTG CAGTGGCGAG ATCTCAGCTC ATTGCAATCT CTGCCTCCCA 780
GGTTCAAGCG ATTCCCCTTC CTCAGCCTCC CAAGTAGCTG GGACTACAGC GGCTAATTTT 840
TTGTATTTTA GTAGAGACGG GGTTTCACCA TGTTGGCCAG GATGGTCTTG ATCTCCTGAC 900
CTCGTGATCT GCTCGCCTCA GCCTCCCAAA ATGCTGGGAT TACAGGCATG AGCCACCACA 960
CCCAGCGCTT TTTTTTGTTT TTTTGTTTTT TTTTTTGAGA CTGAGTTTCA CTCTTGTTGC 1020
CCAGGCTGGA GTGCAGTGGC ACGATCTTGG CTCACTGCAG CCTCCACCTC CCAGGTTCAA 1080
GCGATTCTCC TGCCTCAGCC TCCCGAATAG CTGGGATTAT AGGCATCAAC CACCACGCCA 1140
GCTAATCTTT TGTATTTTTA GTAGAGATGG GCCACTATGT TGGCCAGGCT GGTCTCGAAC 1200
TCCTGACCTC GTGATCCGCC CACCTCGGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC 1260
CACTGCCCCT GGCCCTAATT TTGTATTTTA GTAGAGACGG GGTTTCACCA TGTTGGTCAG 1320
ACTGGTCTCG AACTCCTGAC CTCAGGTAAT CTACCTGCCT CAGCCTCCCA AAGTGCTGGG 1380
ATTACAGACG TGAGCCACTG TGCCTGGCCT TCCTGGCCTG CTTTCTAATC TCATATAGGT 1440
TCATTTTGTT TCCCCATCCA TTAGGGGAAA CTCTGTGAGT AGCCACTGTG ACTCTACTTT 1500
TGTGTCCAAA AATAGCCATT GTGTACTTGA ATGAATGAGG TTCAAGAGCT TAGGTAGCAT 1560
AACCTATTAA TAGTAGGCAT AGAACTTTTA ATAAACTAGA CTTGAGAATC CGACATAGTT 1620
GCACCCATAC TGGCAATTAT CATAGGAGCT TCTGTTCTGA GTCTTACAGA CAGTGCATTA 1680
AAGCTATACA TTGAGATCTA TTGTGCAGGA CACTTTGCTG ATTCTCAAAA AAAGAAAGGC 1740
ACAGCTCTTC TAGAATTGTC ATAAAGGAAA CAAGACTCAA GCTATGTAAT AAAAATGTTT 1800
GCAAAACATT TGAATTAGAA CAGCTTGTTC TGAGTGACAG TCTAATATAC GTAGGAGAAA 1860
TTTTAGAAAG GAAGAGATTT AGGGATTAAA ATTTTTGCAT CAGGGCAAGC TAGTTTTTGA 1920
AGGCATTAAG GGGTGGAATT ATCAGAAGGA AAGAGGAAAG TAATTAGAAC GAAAGAAATG 1980
TTAGAGCTGG AACAGGTTGC CCTCCTGTTG GCAGGTGTCC ACCTGCAGAA CCAGTCTCAC 2040
CTTTCTTTGC TACAAAGGGG AGTCAGTCCT ACATGACTAT AAGGTTGCTG GCCACGAGGC 2100
ACTGTTTTGC TCTTTATCCT TTTTTTCTAA TTCCTGATCT GGCCTATATT ACCATCTTAC 2160
ATCACTCTAG CTCTGAAATG TTTGGCATGC CTACTTTATT TTCTTGTAAT CTCTGTACCC 2220
TCCCTGAGGT CATCCATGAT TTTCAGCTAA GAGGACAATT TTGCAGCTAT TTCTATAAAA 2280
AAAAAAAAAA CAACGCAGTC AGGTATACAT TTTATTGAAA ACAATTACAG CGGAGGGGAG 2340
AGAGATTTAA TTCTTTAGTC CACGTTTGTT AAGAGCATGA GTATGCCTAT ATTTCGGGAT 2400
CAGCTTTTGG ATGAGGATCC TATTCAAGAA TTGATCGTAA TACTGTGTTC TGGGTTTTCT 2460
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