Tag | Content |
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EnhancerAtlas ID | HS047-28119 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr5:178265490-178266650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr5:178266543-178266562 | CAGTGCCTCCTGGTGGTCA | - | 7.46 | TFAP2A | MA0003.3 | chr5:178266298-178266309 | TGCCTCAGGCA | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I178839 | chr5 | 178266401 | 178266550 |
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Enhancer Sequence | AACAAAATCA GTCTCCAATT ACAGGGGTAA GGGAAGATTT TCATCAGTAC CAACTGTTGC 60 ACTGGGGAAG AATCCAGCCT GAGCTGGACT GAACTTGGAT TTGTAGAGGT GACTTTGAGT 120 TTCAAAGGGA GAATGAGGGA ATAAGGAAGG GGTTGGGGGG CGCTCAGTAG AGTCAGGAAG 180 GTGACAAATT GCAAAGGGTT GGTTGAGTGC TGTTGGCCCC AGTGCTGCTC CCGGTCTGGA 240 AACTGTCATC CTCCCAGAGG GACGGGAGAC AGAGGCCTTG TCCCAGGTGC CAGCCAGAAC 300 AAACTACATC CCTTTGGCAG CATCCAGTTT TCTCAGGCAG GCAACTAAGG GGCGCCCGCG 360 TTATCTGAGG GGTGTGGCCT CCAGCGCTGG TAACTGTTAG TGTTTGCTGA AGTCTCCATA 420 GGCCAAGGCT GGGTGGGGCC TGGTGGAGAA CGGGGCTCAG AGGGGCCTGG CTGGAGTCCG 480 GTCCAGGACG TTCTTTGTCA AGAGAGCGAG TTAACCGGGC CCTGGGAGCC TCCATTTTCC 540 CTTGCATATC TGTGAGGAGC AAGAGATGAC GTGATCCAGG AGCCTCCCGG CTCCACATCC 600 CACAGACGCC CTTTCTGATA AAGGAGCCGG GCGGGCACCG CGACTGCGCC CACTGGAGGC 660 CCTGAAGTAG CAAGGCTCCT GGAGCGCGTC CTGCGCTGGA GTCCTGGAGG ATGCCACAGA 720 TCTGGAGGGG GTGGTGGGGT CCTGTCCCAG ACTCGCCTTA AACGCTGCGA GGACAACGAC 780 CCCCCCAGCC CGCCTCCACC CTCCAGCCTG CCTCAGGCAG GAGGCGCAGT AGTCCCCTCT 840 GCAAGCTGCA GATTCCCCAC CCTGGCTCCA ACTGACCATA GTTGAAATCG AGCTGGAGGC 900 GACAACAACA TCCTAGAAAC CTGAGTCCCC GCCTCAGGGT ATTGATGCCC TTTACTGATT 960 GTAAAGCCAG TGTGGAACTC TGCAGCCTTG GCTCAGAAAC GCAGCTGCTG AGTGTCCTGG 1020 AGCAGGTGCG ACCAGAGGAC ATTGGCAGGG GAGCAGTGCC TCCTGGTGGT CAGTGCATGC 1080 TGGCCTCAGT GACGGGAGAA CCTTAAGGCT GGTGACATTC AGTACCCAAG CAGGCAAATC 1140 ACAGAGGTGG CTGGGGGTGT 1160
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