Tag | Content |
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EnhancerAtlas ID | HS182-21582 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr9:80129710-80131190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr9:80130568-80130585 | TGCTCTTGAGGAATTCA | + | 6.28 | Foxd3 | MA0041.1 | chr9:80130506-80130518 | GTTTGTTTGTTT | + | 6.32 |
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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 |
GH09I077514 | chr9 | 80129198 | 80131135 |
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Enhancer Sequence | AGTGGAGACG GGGTTTCACC GTGTTAGCCA GGATAGTCTC GATCTCCTGT CCTTGTGATC 60 CGCCCACCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCAT GAGCCACTGC GCCCAGCCCA 120 GATTTCTTAT TTAAGACAAA TAAATGAAGT TAGCTATTTA TGAGTACAAA GGAAATCAGT 180 TTCAGGACGT TCAGGCAGAT GGAGGATGTG AGATGACAGT GAGGCCTGGG AGAAGCAGGA 240 AACCACAATC CAATAGGGAG AGGAAATGAG GCTGGACACT GCGAGAGACA CGTTCAAGAA 300 AGGCCAGAAT GTGGCCTTAA GGTCAACTGC ATGGGCTCAT AAAAAAATCA CATTCCTTTG 360 CCCCAGGAAT GAGTTCTTCA GTGGATAGGC TTTTGGCAAA CTGGCCTGCA TCTATGTCAG 420 GCACTGCAGC TACAAAGGTG GGGAAAAGTA GGCATAGACC TTGGCCTTCA TAGATCTTCC 480 ATTCTAGTGG AGGACAAGAA AGACGTGGGC AGGCAAAGAG GAAAGGGAAG CAGAGAGAGG 540 AGCATGTGGA AAAGTCCTGG GCTTGAAGGA GCATTGTGAA TACAGGGACC AAAAGAAAGG 600 AGGTCACTGT GGTTGAAGCT GAATGAGCAT GCGGCAGAGC CGGGCAGCCA CTGCTGCCAA 660 AAACCACAAG GCTTGCAAAA ATAGTAAAAG AGAGGCTGTT GATCTGCTAT TGGGTTCCCC 720 GCCCTTAAAA TGCCAAAACT ATGTTATAAT AACTTGAGAT TTCTAATGGT GTTCATCTGG 780 AATTCAAAAG GTATTTGTTT GTTTGTTTAT GCATTGCCTT TGTCTGAGAG CTGGAGGAAA 840 CAGACAGGAA TACAGCATTG CTCTTGAGGA ATTCAAGAGT GAGCTGGTGC CAGTTTCTGT 900 GGCTCACGTC AGTAATCCCA ACACTTTGGA AGGCCAAGGT AGGAGGATCA CTTGTGTCTA 960 GGAGTTCAAG ACCAGCCTGG GCAACATAGG GAGACCCCAT CTTTACAAAA AAATAAAAAA 1020 TTAGCCAGGC CTGGGGGTGT GCACCTGTAG TCCCAGTTAG GAGGCTGAAG TGGGAGGATT 1080 GCTTAAGCCT GGGAGGTCGA GGTTGCAGTG AGCCATGATC ATGCCACTGC ACTCAACCCA 1140 GGCAACGCAG CAAGACCCTG TCTCACAAAA AAAAAAAAAA AAAAAAAAAC CCAGAGCAGG 1200 AAGAGACAGC CATGTAACAG AGTTTCACAC TATGGGGAGA GATGGGAACT AACAGGGGCA 1260 GGTGGTACAT GACCCGCAAG CAGAGAGTCA CTGAAGACTT AGAGGTCTCC AGGAAACCTT 1320 TACTCAAGGA TCTCCTTCAC AAGGCAATGG ACCATTAAAT CCTCGAAGCT TTGTAATATC 1380 AGACTAGTTG CCCATTTTGT CTTCTCTTGG GCCCAATCTT TAGAAAGCAC TCTTAGCTTG 1440 TGCTATTCAT TTCATTCGTA TAACAAATAT TTATCAAATG 1480
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