Tag | Content |
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EnhancerAtlas ID | HS047-28150 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr5:179603800-179605060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr5:179604506-179604517 | CTGCAGCTGTC | - | 6.62 | Tcf12 | MA0521.1 | chr5:179604506-179604517 | CTGCAGCTGTC | - | 6.14 | ZNF263 | MA0528.1 | chr5:179604095-179604116 | GGAGGAGGACCAGGGTGAGAG | + | 6.51 |
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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 |
GH05I180176 | chr5 | 179603796 | 179605111 |
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Enhancer Sequence | CCGCCTCGGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CCACCGCGCC TGGTCCCGGG 60 GCTAATACTT TTTTCCAGAA AGATTCAGCC ACAGCAGAAG CTATGAAAGC ATGACTGCTG 120 CGTGGTGCCA GCCGTCAGGG TTGGGCAGTG GTCAGTCCTG CCCATGTCTC CCCCTGGCAT 180 AACCCAAGAC AGGGCCCCTG GCCTGGCCTC CAACTCCCAC CCAACCTTGG TCAACCTCCC 240 AGAGGAGAGG GCTGCAGACG AGGGGTTTCC AAGGGACGGC AACTTTTGCC AGCATGGAGG 300 AGGACCAGGG TGAGAGGTGA GACTCTCAGA GCCTGACGGA GGGGCTGGAT GAGGGGCAGT 360 GGGATGGGGG GCTGGCTGGG CTACTTCCAG AAACGTCCAG CCGAGTAGAG GATGCATTCA 420 AACCATGTGC ACATCAGCCC CTCAGCCCCG AAGCCAGGGG CTGCTTTCCC TTTCCGGCCC 480 CACCTCCCCA CCCAGTGAAG GGGCTGGCCT GCCCGGCTCA CCCAGCAGCT TCCCCAAAGA 540 CACAGGCTGT TCATCGGCTC CATTTTTAAC CTTCCTTAGT CCCAGCAGCC CCAGCAAAAG 600 CTCTTCGGTG AGTGCCTGCG CAATCTGCCC GGCTGGGCCG CAGCAGTCCA CGGGCAGGGC 660 AGAGCCCCGG GCTTCCTTCC GGGACCCCTG CCAAGGCTCA GCCCTGCTGC AGCTGTCCAA 720 GGCCATGGCC TCTGCGGCTT CTGCCTGGCC AGCATCTGTT CTTCCCTCTG AAAACAGAGC 780 CCATTTGTCC TTCCTCTCCT GCCCGTGGTA GGAGGACATG GCCCTGGTGC CACTTGGGGA 840 AGGAGTTGCG TTGGTCTGTG ACAGTTGGGA TGGCATGTGA TCCAGGCCCA GCCACTCAGT 900 GCCTTTCATC TCCCTGGCCT CTGGGATAAA TCCATGGGCA GGCATGTCAC CTGGGTGGGC 960 CACCAGACTC AGTTCGTGGG ACATTTATTT GAACTGTCTG AGCAGAGCCT CTCTCTCTGC 1020 TCAGGGCAAG GTAAGGACAG GAAGTAAGTA TGGAGCTGGT GGGGGCTTTC TTGTGAAAGG 1080 GGCCCACATG GAGGAAACGG AGCCAAGACT CACAGAGACC GAGACCATGT CCCACATCCA 1140 GCCATGCCTG AAGCCCACCT TGGGCTTTTT TTTTTTTTCT TTTTGAGGTG GAGTCTCGCT 1200 CTGTTGCCCA GGCTGGAGTG CAGTGGCATG ATCTCGGCTC ACCGCAACTT TCGCCTCCCA 1260
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