Tag | Content |
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EnhancerAtlas ID | HS047-06019 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr11:61279700-61281180 | 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 | CTGAGTAGCT GGGATTACAG GTGTGCACCA CCACGCCCGG CTGATTTTTT TGTATTTTTA 60 GTAGAGACGG GGTTTCACCA TGTTGGCCAG GCTGGTCTCG AACTCCTGAC CTCAGGTGAT 120 CTGCCTGTCT CGGCCTCCCA AAGTGCCGGA ATTACAGGCG TGAGCCACTG CACCTGGCCC 180 AAGGAATTGG GTTTATTTAG ATCTGATGCT GCAGCTCAAT ACTTCATGCA AGGGGTTTGT 240 TTACCTTCCT TTCATGCAAA TCTTAGACAC AGAAGCAGCA GGGTGCAGAG GCAGCCATGG 300 TCACCTGCAA TAACTGCTGT CATTAGTGAG CTCAGGTCTC CTCCCTCTGT CTGATCTGTT 360 TCCCTGTACC TCCTCCCCTG CTGCTCTCAC CTGAGGACTC TAGGTTGGGG CAAAGTCCTG 420 GCAATGAGTC CCCCGGGCCA TCCTGAGGCA CTCAGGGCCT TACCCTTTTG CTTTGTCAAA 480 CGTGGCACCC GCAGCCATGA CTGCTTGCCA GCTGAGCAGG CGCTCCCCCA GGGAATGGGA 540 ATGGGCTCTG TCCCTGGCCC TGCTACTCAC TTGCTCTCCA CCCTCAGAAG CCAGTCCCTT 600 CTGGAAAGTT TGAGTTTGGC TAAATTGGGT GCTGATGCTA CAGAGCACGA TTGAGGGTCT 660 CTGTCTCCAT GTGAGTAGGG AGGGAGCTAA CTGCCAGGGA AAACTGGGTG TCACGGCTCC 720 CCTCGGTGAT GGAGATAGCA CTGTATTAGG AGTCCTAGCA TTCCCCCACC CACAACTTCC 780 TGTGATTCCC ACTTGGCCTC TGGGGAGTAG GGGGCAGGGG AGACTGGAAG GGACGCTTGT 840 AACAATGGGA CGGGATGGAT GGGCTGCCTC TGCGGTTCCC CACATCGTCC TGGGGCAGTC 900 AGAGGTGGGC AGGCCATGGG GGAATAGGGC AGGGAAGTTC TGCAAGAGTC ATGTTTGTAC 960 CAGGGATTCA GGGGCAGAGG CCAAGGGCGC TGGTGGTCAG AGCAAGAAGC TTCCTTCCTA 1020 CTGTGGGAAC CAAGTGGAGG GAAAGGCAGA GGAGGCGGCA GGGCAAGAAA CAGGGTTGGG 1080 GGGGGTGTGG GCGCGAGTGA CTCACCCGTA AGCGGTGTGA GGACTCCCAA CCCAGTGCTC 1140 ACTGTGTCAC AGAAGAGCTG CTTGGTCCCT GGCTGGCAGT CAGGTCTGTG AGTGGAATGG 1200 AATGGCTGAG AACTGCGCCT GTTCTTGAGG CCCCCGCCCC CACCAGCCTC CAGGCAAGCA 1260 GCCCTGCTGG CCAGTGTGGC AGCAGAGACC CAGGCCTGGA GCCTTTTCTA ACCTTGTGAA 1320 TGCCATTCCT CACCCCCTTC CCACCCACCC TCATGGGACT CAGGAAAGTG GGAGAACAGG 1380 TTCTTGGAGC TGGGGGCCCT ACCCAGAAGT CCCTCCCTGC CTCCCATGCC ACCACACTGG 1440 CTTACTCAGC CATCTGTCCC AAAGCTTCCC CAAGACACCT 1480
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