Tag | Content |
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EnhancerAtlas ID | HS050-02187 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:48058250-48059790 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr1:48059587-48059598 | CCACACCCTCC | + | 6.32 | TCF7L2 | MA0523.1 | chr1:48058415-48058429 | CAAGATCAAAGGGA | + | 6.83 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTGCCAGGT GAGCAGTTTT TGGAGCTGGC ACAGTGCTCA AAATAAAATG AAACAAAACC 60 TGGACTGGAA CTCAGGAGTC GTGGGCCTGT CGCAGACCTG CTGGTGATCT TGAGTAAGCC 120 CCTTGCCCAC TCTGGGTGCC GAATGGATGA GCCTGGATGC CCTCTCAAGA TCAAAGGGAA 180 CGATGAGGCC TGTCTGATCT CCCAGCTTCA GAGGCAAAGT CCTGTGACCC ATTGAAAGTA 240 ATTTTATCTC CCAGCTCCTG AGCGCAGGTG CTGAGTGGGA TTCAGTGAAG GGCTGGCGCA 300 CGGGGAGGGC ATCAGGAAGT GCTAGAGGAA CTGGACTGGG GACTGATCCC CTGGGGCTAC 360 TGAGTCTATG CCCCAGGTAA CTGGCTGGGC ACAGACTTCA TCCCCAGGCT CTGGGAGAGA 420 GAGGGGGAAG GGGAGGCAGG GCTGCCACTA GCCCTTAGGA CTTGTTCGTG CGAATTAGAA 480 CAATTAGAAA AAGGCGCTCA GTGAGTGGAG CATCCTGGCA AAACCGGACT GGTGAAGGTT 540 CTGCGCGCGT CTGCCAGGTG CCAGGGAAGG TCTCCCAGCG GTCTTGCGCG GAAGGCGTTA 600 TCAGCCCCGC TTATTAGATG AGGCGGCGCC TGCAGTAGAG GGGGCCGTCT CCGCAGGGTC 660 TGCAGCGCCG GGGCCCGCAC CTCCTGCTCC GCGGCCCGCC GCCGCCAGCC CGGGGCTGAC 720 CTCTCAGAGC AGGGCGGAGG ATTTTCACAG CACAGCTTCC CGAGAGAGCG GGATTAAGGG 780 GGAACTGCTC GGGTGGGCCA GAGCCAGGGG CTAGGGGGAG GCCGGGCGGA AACCCAAAAC 840 CTCCGCAGCT GTTTCCAGTT TGCCGCCCTG GCTGGACCGC GGTGGCTGCG TGCAGAGCGA 900 GCAAGGCTGC GCGGGCCTGG AGCGCCCACG GGGCGCGGGA CCTCTCTCTG TCTCCCCCCG 960 CCCCGCGGGG CTCTCTCTCG TCCTCTCTGT CTTGGTGGGG CTCAGTCTGT CTCTCGTTTT 1020 CTCTCCCTGT TTCTAAGATC TCGTGGAATC AAAGACATTT TGGAGGTCTC TGGTCCATCT 1080 GAAAGGGGGA TACTGGGTTC ACCCGATCCC ACGCTTTGCC TTCTAGAGCT TGCTGCCCTG 1140 GACACCCCCC ACCCCATTCC CCCACCCCGA CCCCGCCCCT CGGCCCCCAG CTCCAGGCCC 1200 GCCAACCCCG CCAACCCCGT TGCACTCCCA TGCAGAGAGG TGGCCCTCCA AGCCCAGGGT 1260 TCAGAGCTCA GGTCAGGAGT CCTGGCAAGG GCTTTGGGGA CAGGCTTTGC CTCCCAGCCA 1320 AACTCTGCCC TTCAGGCCCA CACCCTCCTC TCCTGGGCAT CTTTTCCACC TGCCTGCACC 1380 CCTAAGCCCC AGGCTTACCC CATGGGAGTC CCCATGAAGG TCCAGGGTCC CAGCACTGAC 1440 TTTATACTCT AGGCAGAGGC AGGAAACCTC CAAGCCCCGC TCCCACCCAG GAGTCAAACC 1500 CTGGAGACAG CTCAGACAGA GATTGAGCAG TAGTGGAGGA 1540
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