Tag | Content |
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EnhancerAtlas ID | HS042-01579 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr1:48058500-48059760 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr1:48059587-48059598 | CCACACCCTCC | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCAGCTCCTG AGCGCAGGTG CTGAGTGGGA TTCAGTGAAG GGCTGGCGCA CGGGGAGGGC 60 ATCAGGAAGT GCTAGAGGAA CTGGACTGGG GACTGATCCC CTGGGGCTAC TGAGTCTATG 120 CCCCAGGTAA CTGGCTGGGC ACAGACTTCA TCCCCAGGCT CTGGGAGAGA GAGGGGGAAG 180 GGGAGGCAGG GCTGCCACTA GCCCTTAGGA CTTGTTCGTG CGAATTAGAA CAATTAGAAA 240 AAGGCGCTCA GTGAGTGGAG CATCCTGGCA AAACCGGACT GGTGAAGGTT CTGCGCGCGT 300 CTGCCAGGTG CCAGGGAAGG TCTCCCAGCG GTCTTGCGCG GAAGGCGTTA TCAGCCCCGC 360 TTATTAGATG AGGCGGCGCC TGCAGTAGAG GGGGCCGTCT CCGCAGGGTC TGCAGCGCCG 420 GGGCCCGCAC CTCCTGCTCC GCGGCCCGCC GCCGCCAGCC CGGGGCTGAC CTCTCAGAGC 480 AGGGCGGAGG ATTTTCACAG CACAGCTTCC CGAGAGAGCG GGATTAAGGG GGAACTGCTC 540 GGGTGGGCCA GAGCCAGGGG CTAGGGGGAG GCCGGGCGGA AACCCAAAAC CTCCGCAGCT 600 GTTTCCAGTT TGCCGCCCTG GCTGGACCGC GGTGGCTGCG TGCAGAGCGA GCAAGGCTGC 660 GCGGGCCTGG AGCGCCCACG GGGCGCGGGA CCTCTCTCTG TCTCCCCCCG CCCCGCGGGG 720 CTCTCTCTCG TCCTCTCTGT CTTGGTGGGG CTCAGTCTGT CTCTCGTTTT CTCTCCCTGT 780 TTCTAAGATC TCGTGGAATC AAAGACATTT TGGAGGTCTC TGGTCCATCT GAAAGGGGGA 840 TACTGGGTTC ACCCGATCCC ACGCTTTGCC TTCTAGAGCT TGCTGCCCTG GACACCCCCC 900 ACCCCATTCC CCCACCCCGA CCCCGCCCCT CGGCCCCCAG CTCCAGGCCC GCCAACCCCG 960 CCAACCCCGT TGCACTCCCA TGCAGAGAGG TGGCCCTCCA AGCCCAGGGT TCAGAGCTCA 1020 GGTCAGGAGT CCTGGCAAGG GCTTTGGGGA CAGGCTTTGC CTCCCAGCCA AACTCTGCCC 1080 TTCAGGCCCA CACCCTCCTC TCCTGGGCAT CTTTTCCACC TGCCTGCACC CCTAAGCCCC 1140 AGGCTTACCC CATGGGAGTC CCCATGAAGG TCCAGGGTCC CAGCACTGAC TTTATACTCT 1200 AGGCAGAGGC AGGAAACCTC CAAGCCCCGC TCCCACCCAG GAGTCAAACC CTGGAGACAG 1260
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