| Tag | Content |
|---|
EnhancerAtlas ID | HS121-09872 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr12:133295750-133297260 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT1 | MA0137.3 | chr12:133296503-133296514 | TTTCCCAGAAA | - | 6.02 | | STAT3 | MA0144.2 | chr12:133296503-133296514 | TTTCCCAGAAA | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAATTTGCCT CTTCTCTGGA TCCATTAGGA AATGTGTGTG TGGGCTCCGC AGCTGAGGGG 60
GCCCTCTTGA GTGTGACGAG TCCTGTGGTG GGAGGACAGG ACGGCACTGG TCAGTGATGC 120
CGTGTGAGGC TGGGCCCTGG TCTCTGCCCG TCTGTCACCT GGGCCTGTCA CCAGGGCTGG 180
GGCTGCTGGG AGCACCATGG TCAAGAGCAG CAGCTCCCAG AAAGTCGAGG ATGTACGGGC 240
CGAGATTCTC AAGCTTGGCT CCAGACCAGA TAGAGCTTTT CTGGGGGTTG GAGCCTCCGG 300
GTGGTGTGGC CTCAGGCTAA GTGAGTACCT GTTTGCTGTG AGTCGTTCGT TGCCTCCTGT 360
CTGTGCTTGT GAATGAGCCA TATGGGTGGC TTCTATGCTG CCACCACCAC CTTGTGTGTC 420
CATGACACAG TCACCCCGAG GTGACACAAA TGCTAAAAAT GCACAGAAAT AACCGGGGCG 480
GGAGAGTGGA GCCGACCTGA GTCCACACAG TGGTGAGGGC CAGGCACGTG CACCTGGACA 540
CGAGAATATG GCTGTGCTGT TCCGGCCGGT GCCGCCAGGC AGCCCTGAGG AGGCTCGGGA 600
AGCAGCGTGA GGGTGGCCAT GCGGCCCACT GAGACAGGGC GGTGGGTGGC TCAGAGGCGA 660
TGAAGGCAAC TCCGAGCTTT TCCGCAAATG CGAATTGTGC CTAAGAAGTG CATGAAGATG 720
CCACGGCGGG TAGATCCCAT CTCCGTTCTT TGCTTTCCCA GAAAGGGACC TGTTGCACTA 780
ACTGGCTGCT CCCTGCTTTT ATATGGGAAA AGCAGAAATT AAACTGTGTT TCCTCGTAAG 840
AAGTCAGCGT TGTTCTGATC TGTGCAAATC TTGAGTTGGG GTTGGGCCCC TGTCCTAAAG 900
AGGGCAGGTC CCCAAGTGTG ATGGCTCCAT TCATGTCGAT CCCAGTCATC GATTCACGTC 960
GATCCCAGCC AGATCTTCCC CGAGAAGCCC CGACTGAAGA CAGGAGCGGC TCGGCTGATG 1020
TGTACCCCGG CCCTGAGGCT GCTCTGAGAC TTCTGAGGGG CTCAGCCTCT GTTTGTAGAA 1080
CAGAGCCCCC TGGCACAGCC TGGCCCAGCC TCTTTTAAGG ACAGAGTCCC CTGGCTCTAG 1140
CCCAGCCCGT TTTTTTTTTT TTAGACAGAA TCTCGCTCTG TCACCCAGGC TGGAGTGCAG 1200
TGGCGCGATC TCAGCTCACT GCAAGCTCCG CCTCCCGGGT TCACGCCATT CTTCTGCCTC 1260
AGCCTCCCAA GTAGCTGGGA CTACAGGTGC CTGCTATCAC GCCCAGCTAA TTTTTTGTAT 1320
TTTTAGTAGA GATGGGGTTT CACCGTGTTA GCTGGGATGG TCTCGATCTC CTGACCTTGT 1380
GATCCACCCG CCTGGCCTCC CAAAGTGCTG GGATTACAGG TGTGAGCCAC CATGCCCGGC 1440
CTAGCTCAGC CCGTTTTAAG GACAGAGCCC CCTGGCTCTA ACGTGCTCTT TCTCTCTCTC 1500
TCTCTCTCCC 1510
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