Tag | Content |
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EnhancerAtlas ID | HS182-06107 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr13:113829780-113831440 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr13:113830277-113830288 | AATGAGTCACC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr13 | 113829788 | 113829838 | chr13 | 113830223 | 113830631 | chr13 | 113830669 | 113830857 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I113175 | chr13 | 113829957 | 113835615 |
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Enhancer Sequence | AAGTCAAAAG TTGAAGGATG TTCAAGGCCC ATGCAGAGCA GCAGGGAAGA TCAGATTTCC 60 GTACCCAACA CTGCAAGAGA ACGGGGCCCC ACTGGACACA TGGGTAGCTA GAAAACAGAT 120 GCGCGCCCAA AGCCTCCGCC GGCATGAGTT TGCTCCGTGT CTGCCCCACA GGACATAGGA 180 GGCACTTGTC ACGACTGCCA GCGCTGAGGA CCTTGCTGCT GCTGGGGAGC AGCTACGTAG 240 GTCAAGAGGA TCCTTGGCAT GAACTCCACA GGCACAGGCG CTTGCCTTCG TGCATTCATC 300 TCTCGCGTGT ACGTGTGGCA GTCCACGGCT GGAATCCGGG TGTGACTTAG GAGAGCAGGG 360 CATAAAAGAG ATCTGGCTTC CCTGGCTCTA CTGGGATCTG CGCTCCCAGA ATCCAGCTCC 420 CTACGTGTGG AGAGAAACAG GGGAGCCCAC CCACAGCCCT GCTGAGCTCC AGGTGAGAGC 480 CCGGGCCAAT ACACGGGAAT GAGTCACCTT CAAAGAGGCC CATTCGGGCC CCAGAAGAGC 540 CCACAAGCTT CCCCGCCCAG CCCGGAAGAA ACTGCAGACC TGCAGATGTA GGAGCGAGCT 600 AAGGAGTGCT GCTGAAGCCC TGGGGCAGCT CCTGCATCCA GGGGAACCTG AGGAAGGAGC 660 CACACAAAGT GAGTCCTGCG CCGCGCGGCC CGGAGAGAGA GAAAGAGGGA TTCACACTTT 720 GTAGAATAGC CTCTCCTTGA ACAAGCAGCT TTCAAATGCA GTAACTTTGC AAAGATGAGC 780 TCTTATAGTT TGTGTTCTTC TTTAGTAAAT TTTTTATAAA CGGGGAAATG TGCATAGTCT 840 GAAAAATGGC AGTGCTGGGG ACTAAACTGT GTCCCCCAAA TTTCTTACAT TGAAGTCCTA 900 GCCCCAGTGT GACTGTATCT GGAGGTAAGG TCTTCAGGGG GTAACTAAGG CTAAATGTGG 960 TCATAAGGGT GAGGTCCTAA CCCAACAGAA CTGTGGCCTT ATAAGAGGAA GAGAGCCGGG 1020 TGTGGTGGCA CATGCCTGTC ACCCCAGCAC TTTGGGAGGC CGAGGTGGGG GAATTGCTTT 1080 AGCCCAGGCG TTCCAGACCA GCCTGTGCAA TATTAGCAAG ACGCTGTCTC TACAAAAAAT 1140 AAAAAAATTA GTTGGGTGTG GTGGCATGCA CCTGTGCTCC CAGCTACTTG GGAGGCTGAG 1200 GAGGGAAGAT CACTTGAGTC TCGGAGGTCG AGGCTGCAGT AAGCACTGAC TGCACTGCCG 1260 CACTCCAGCC TGGGTGACAG AGTGAGGTCC TGTCTCAAAA AAGGAGGGAG AGAGTCATCT 1320 CTATCTGTAC CATCTCTAGC ACAGCAAGAA TACCACCTTA TTCTTAAGTG TGCAACTCAG 1380 AAGAGAGCCC TCCCCAGAAG CCGACCGTGC TGGCAACCCC ATCTCAGTCA GACCTCCAGC 1440 CTCTAGAACT GTGAGGAAAT ACATTCCTGT TGCTTAAGCT GCCTGTGGTA TTCTGTGATG 1500 GCAGCCCCAA CAGCCCAATG TGAGTGGCCC AACTTAGCGA CTGTCAACCT CGCCGTGGTG 1560 CCGAAGGGAC GCGCTCAGGG GCAGCCATGC CTCAGCGTCC ACGCAGCCCT TCAGTTTCCA 1620 CTCTCAGTGT AGCACTCGGT AAGCTACACG AGGTATTTAC 1660
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