Tag | Content |
---|
EnhancerAtlas ID | HS121-06665 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr11:61278490-61281180 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chr11:61279935-61279949 | TTTGTTTACCTTCC | - | 6.18 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGTGCATTTC CCATGTGCCT GTTTATTTAT AATCCCTGGG AGCACCGGAA CCCACTGCTG 60 TGGGGACCCT GGGCTCCCTC TGGCACTGCC CCCGCCCCAC GTGCTCCCCG CTCCATGTCA 120 GACCGACCCT GCCAACTGTG GTGTGCTGTC TGTCTGGGGA ACAAGTGCTG TCGTCAGAAG 180 TGGCTTTTGT CCCTCGAGGC TGCTCTCCTG TCTTGCGGAA TCCCGCAGCT TAATTCTGCA 240 GAAGATTTTG TATGTTTTTG AGTCACCCTC GAGCTGGGCC GATGGTTCCC TACTCTTTCA 300 CTGGCACTGC CCCTCCACCC CCTCCATGAC TCTAGACTCG CCTCCCTCCG TCTCTCTCGC 360 TCTATTTTCC TCTTTCTGTC TCTCTCCTTC TTAGTCTCTT TTTGCTCAGT TTTGGCATTT 420 CTTTCTCCCC TTGTTGTTCA GGAAAATAAT AAATTAACGA TTTAAAGAAA GGAAGAAAGT 480 TGTAAAACCC AAGCCTGGAG GCCCATCTCC CCGGAGAAGA TCCTGCCAGA TCTTCATCAC 540 CATGGCAACA GGGGCATATG GGGCCAGAAG GTCAGGCCCT GCCCAGCAGC TCTGCTGGCA 600 CACTGGGCTG GGCCCTGGCT AAGGAGGAGG CTGGGCATGG GTCTGGGGCT GTCAGCTTGC 660 AAATGAGAGT GAAGGCCTTG AACGGACAGA AAGAGGTGGT GGGTGGGGAA GATTGGAGAC 720 TGCCACCTTC CCAAGGAGGA AGAGGGTCTG GGGCCTGGCT GCTGTAGACC TTGTCCCTCC 780 CAGAGTTCCC CCTGTTGGGG TTCCATCAGG GCCAGTGGGC CTTTCAGGGG TCTGGAAACT 840 TGGAGAAAGT AATTTGAGAG AAGATCACTC AGGTGGGGTA GGAGCTGCAG CTGACTGGGG 900 ACTCTCCTCT TGACCTGCCA CTTGTATCAC AGCATAGGGA AAATACCCCT GGGCCTACAA 960 TCAGAAGGCA GGGGTTGCAG GCCTGGTTCT GCTATTGACC AAGTGATCTT GAGCAAGTCA 1020 CGACCCCCCT GGGCCTTAGC TTCTTCGTCT GTACACGAAG AGTTGGGTTT ATTTATTTAT 1080 TTACTTTACT TTTATTTTAT TTTCCAAGAT GGAGTCTCTC TCTGTTGCCC AGGCTGGAAT 1140 GCAGCAGCAT GATCTTGGCT CACTGCAACC TCAGTTTCCC AGGTTCAAGC AGTTCTCCTG 1200 TCTCAGTCTC CTGAGTAGCT GGGATTACAG GTGTGCACCA CCACGCCCGG CTGATTTTTT 1260 TGTATTTTTA GTAGAGACGG GGTTTCACCA TGTTGGCCAG GCTGGTCTCG AACTCCTGAC 1320 CTCAGGTGAT CTGCCTGTCT CGGCCTCCCA AAGTGCCGGA ATTACAGGCG TGAGCCACTG 1380 CACCTGGCCC AAGGAATTGG GTTTATTTAG ATCTGATGCT GCAGCTCAAT ACTTCATGCA 1440 AGGGGTTTGT TTACCTTCCT TTCATGCAAA TCTTAGACAC AGAAGCAGCA GGGTGCAGAG 1500 GCAGCCATGG TCACCTGCAA TAACTGCTGT CATTAGTGAG CTCAGGTCTC CTCCCTCTGT 1560 CTGATCTGTT TCCCTGTACC TCCTCCCCTG CTGCTCTCAC CTGAGGACTC TAGGTTGGGG 1620 CAAAGTCCTG GCAATGAGTC CCCCGGGCCA TCCTGAGGCA CTCAGGGCCT TACCCTTTTG 1680 CTTTGTCAAA CGTGGCACCC GCAGCCATGA CTGCTTGCCA GCTGAGCAGG CGCTCCCCCA 1740 GGGAATGGGA ATGGGCTCTG TCCCTGGCCC TGCTACTCAC TTGCTCTCCA CCCTCAGAAG 1800 CCAGTCCCTT CTGGAAAGTT TGAGTTTGGC TAAATTGGGT GCTGATGCTA CAGAGCACGA 1860 TTGAGGGTCT CTGTCTCCAT GTGAGTAGGG AGGGAGCTAA CTGCCAGGGA AAACTGGGTG 1920 TCACGGCTCC CCTCGGTGAT GGAGATAGCA CTGTATTAGG AGTCCTAGCA TTCCCCCACC 1980 CACAACTTCC TGTGATTCCC ACTTGGCCTC TGGGGAGTAG GGGGCAGGGG AGACTGGAAG 2040 GGACGCTTGT AACAATGGGA CGGGATGGAT GGGCTGCCTC TGCGGTTCCC CACATCGTCC 2100 TGGGGCAGTC AGAGGTGGGC AGGCCATGGG GGAATAGGGC AGGGAAGTTC TGCAAGAGTC 2160 ATGTTTGTAC CAGGGATTCA GGGGCAGAGG CCAAGGGCGC TGGTGGTCAG AGCAAGAAGC 2220 TTCCTTCCTA CTGTGGGAAC CAAGTGGAGG GAAAGGCAGA GGAGGCGGCA GGGCAAGAAA 2280 CAGGGTTGGG GGGGGTGTGG GCGCGAGTGA CTCACCCGTA AGCGGTGTGA GGACTCCCAA 2340 CCCAGTGCTC ACTGTGTCAC AGAAGAGCTG CTTGGTCCCT GGCTGGCAGT CAGGTCTGTG 2400 AGTGGAATGG AATGGCTGAG AACTGCGCCT GTTCTTGAGG CCCCCGCCCC CACCAGCCTC 2460 CAGGCAAGCA GCCCTGCTGG CCAGTGTGGC AGCAGAGACC CAGGCCTGGA GCCTTTTCTA 2520 ACCTTGTGAA TGCCATTCCT CACCCCCTTC CCACCCACCC TCATGGGACT CAGGAAAGTG 2580 GGAGAACAGG TTCTTGGAGC TGGGGGCCCT ACCCAGAAGT CCCTCCCTGC CTCCCATGCC 2640 ACCACACTGG CTTACTCAGC CATCTGTCCC AAAGCTTCCC CAAGACACCT 2690
|
| |
|
|
|