Tag | Content |
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EnhancerAtlas ID | HS182-04134 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:73265790-73266960 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr11:73266206-73266221 | AGAGTCCAAAGTGCA | + | 6.38 | Klf12 | MA0742.1 | chr11:73266604-73266619 | TAACTGGGCGTGGTC | - | 6.44 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 73266825 | 73266908 | chr11 | 73265934 | 73266000 |
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| Number: 2 | ID | Chromosome | Start | End |
GH11I073554 | chr11 | 73265861 | 73266010 | GH11I073555 | chr11 | 73266161 | 73266330 |
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Enhancer Sequence | AAGGGTGAAA TACAATGGGA GAGCAATAAA GAGGAAATCC CATCAGACTC CCAGGAGGTC 60 ACTTTCATTT CAGAATGTCT GTCATCAGCA AAGCCAAGTT CAATGAGTAA AGAGAGAAAT 120 GAAACTTGAT GGGTGAAGAA GATGGCAAGC TAAGACCCAC TGCTAAAATC CATAAGTTCC 180 TCAAGATCAT GGAACCTGTC AATTACCATA TAGCGTGACA AAGGCCATGG AAGGAAGGCA 240 GCAGCAGGAA TGTGGCAAAG TCAAGAGAAG GTCAAGGTAG CCTTTGTTGA AGATGACTAA 300 TTTAAAGGAG AAAGACATTA GCCTAGAGGA AAAGGGCATT CTAGGAAAAA GGGAGAGCCT 360 AGAGAATAGA AACAGCTTAA CATGCCTTGG GAAATGACAT GTATTTCAGT GTTGCTAGAG 420 TCCAAAGTGC AAGGCAGGCT GTGGTGAAAG ATGTAGTTGC AAAAGTCATC AGGGGCCTGT 480 CTCAGAGGAC CTGAATATCT GGTCTACCAT TAAGCCAAGC AGCTATACAT GAGTCAGTCA 540 ACAAGGGTAC CATTCCAGTA GAAGAGAGAG TTAGGCAGCA TTATAATAAA GATAAGTGAT 600 GGGTGGTTAG AGCAGAAGAG GAACACCCAA TCCAGCCTGG GGGCTCATGA AAGGCCTCTA 660 AGAGAAAATG CCAAAGTAAG GCACAAAGGA AAAATGGGGC TAAGGTCCCA GCACTTTGGG 720 AGGTCGAGGC GGGTGGATCT CTTGAGGTCA GGAGCTCGAG ACCAGCCTGG CGAACATGGC 780 GAAACCCCAT CTCTACTAAA AATATAAAAC AAATTAACTG GGCGTGGTCA TGGGCGCCTG 840 TAAAACCAGC TACTTGGATG GTTGAGGCAG AAGAATTGCT TGAACCCGGG AGGCAGCGGT 900 TGCAATGAGC CAAGATCTCA CCACTGCACT CCAGCCTGGG TGACAGAGTA AGATTCCATC 960 TCAAAAAAAA AAAAAGAGAA AATGGGGCTA AGGGCTGCAA CGTCCAAAGT GAGGACACAC 1020 AGTTGATACC TGGCCTAATC ATAAACTCAG CAAATCAGAG AACTAGTGCC TGGCAAGGCT 1080 TCCAAAGAGG GAACCATTCT TATCAACAGA ATGTAACCTC CAAGGACCTT GTTAGTCTTG 1140 TTCACTGCCA GGCTTCTAAT ACTAAAAATA 1170
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