Tag | Content |
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EnhancerAtlas ID | HS047-18237 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr2:392630-394470 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr2:393131-393148 | TGCTTACCAGGCATTCA | + | 6.09 | BCL6B | MA0731.1 | chr2:393227-393244 | TGCTTACCAGGTATTCA | + | 6.09 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH02I000393 | chr2 | 393341 | 394930 |
| Enhancer Sequence | TGCTTGAGAA GCGTGGATGT ACAGAAGAGA AAGCCTCTCG GGTGGGGTCA CCGCAAAGAG 60 GAAAGGGCGC ACGCAGGTCA CTGCAAAGAG GAAAGGGCGC ACGCAGGCGC AATGCACAGA 120 TCCACGGGCA GCATCTAGAC GACGTGCGCT GCTCACAAGG CGAACCTTCG CTCAATGCTC 180 CGGAAGCTGG TTTCCGAATT CACGCCAGCT CACAACTGAC CTTCATGCTA CACTTTGGGT 240 CCCGTGAGGG CGGCTGCTTC CCCCTGCTCA CTCTTGGGCA GCTGGAGCCT AACATAGAAC 300 CTGGCATGTG GTAAGCGTGT GCTCAAACTT CACGGCGGGG TGAGGGTGCA GGCATGTGCT 360 TACCACACAC TCAAACCTCA CGGCAGGCTG AGGATGCAGG CATGTGCTTA CCACACACTC 420 AAACCTCACA GGCAGGCTGA GGGTGCAGGC AGGTGCTTAC CACACACTCA AACCTCAGGG 480 CGGGCTGAGG ATGCAGGCAC GTGCTTACCA GGCATTCAAA CTTCACGACT GGCTGAGGAT 540 GCAGGCAGGT GCTTACTACA CACTCAAACT TCACGGTGGG CTGAGGGTGC AGGCACGTGC 600 TTACCAGGTA TTCAAACTTC ATGGTGGGCT GAGGGTGCAG GCATGTGCTT ACCGCACACT 660 CAAACTTCAT GGGGGGCTGA GGGTGCAGGC ATGTGCGTAC CAGGTATTCA AACTTCATGG 720 TGGGCTGAGG GTGCAGGCAT GTGCTTACCA CGCATTGAAA CTTCAGGGCG GGCTGAGGAT 780 GCAGGCATGT GCTTACCAGG CACTCAAACT TCACGGCAGG CTGAGGGTGC AGGCATGTGC 840 TTACCAGGCA CTCAAACTTC ACGGCAGGCT GAGGGTGCAG GCATGTGCTT ACCACGCACT 900 CAAACTTCAC GGCGGGCTGA GGGTGCAGGC ACGAGCTTAC CACGCATTGA AACTTCAGGG 960 CGGGCTGAGG ATGCAGGCAT GTGCTTACCA CACACTCAAA CTTCACGACA GGCTGAGGGT 1020 GCAGGCATGT GCTTACCACG CACTCAAACT TCACGGCGGG CTGAGGGTGC AGGCACGAGC 1080 TTACCACACA CTCAAACTTC ACGGCGGGCT GAGGGTGCAG GCACGAGCTT ACCACACACT 1140 CAAACTTCAC GACAGGCTGA GGGTGCAGGC ATGTGCTTAC TAGGCAGTCA AACTTCACGG 1200 CAGGCTGAAG GTGCCTGCTC CCAAGCGATC TCATGCAGCC TGCACTCAAA CTCCACATTC 1260 CAAAAGTACC TACTCATCTG CCTAGATGCC TGCAGGGCTG GCTCTGATCT GCTTGTCCTG 1320 AAATGTGTTA ACTGCCTTTT CATACCTTTT TTCATTGCCA TGCCAACTGT GAAAGACTCC 1380 AGCCCCTTTC AGATGAGGCC CCCAGCTCGG AGATCCACCC TCCAGGAGGT GCTGGGCAGA 1440 CGCGTGGGGC GGCCTCCACC TCCGGTTTCC TCCCTGTTGC CTCCCGCAGC CTCTCATTCA 1500 GAAAGAAACG TGTTTCCGGA AGCTGTGCCG TTGCCATGGA GCCTGGATGG CTTTGTCAGT 1560 TTCCTTATTT GCAGCCTCAT CTCATCTCCA GACCCACTGT GCTCCTGGAC TCGCTGGCAG 1620 TCCCAGCTCT CGCCTTCACT GTGGTCTGTG GACCCCTGCA CTGAGCCTCG TGTCCTGTGA 1680 AGTCAGGCTC TGAGGGTCTC CACGGCCTCC TCTCACCAGA GACCCCCACA TCTGCCGCGA 1740 ATATAACCTA ACACTCGAAA CCTTTCTCAG TGGCTTGTGC CACCTTTTGA ACTTACAATG 1800 TTGCTTTGTA GTTCCTTTTA TCTGTTGTAC GCTTCAGTTA 1840
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