Tag | Content |
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EnhancerAtlas ID | HS182-22566 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chrX:153348020-153349480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chrX:153348022-153348036 | AAAAAATGAGTCAT | + | 6.93 | MEF2A | MA0052.3 | chrX:153348165-153348177 | TCTAAAAATAAA | + | 6.07 | MEF2C | MA0497.1 | chrX:153348163-153348178 | AATCTAAAAATAAAA | + | 6.49 | ZNF263 | MA0528.1 | chrX:153348782-153348803 | GAAGGAAGAGGGCGGGGGAAG | + | 6.06 |
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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 |
GH0XI154081 | chrX | 153347047 | 153349654 |
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Enhancer Sequence | TTAAAAAATG AGTCATACAT AGAAAGTAAG CACATGCTTG AAAGTGCTCA TGTTCAAGTT 60 TTAGCAGCAA TGTGGAATGT TGCAAAAGAG ACAGGGACAC AGGGAAATGT GCATATCTCA 120 GAAGCCTACT TTGCTTTCTT TCAAATCTAA AAATAAAACC TTTGGACTGC CCTATTAATA 180 AGTCTAGAAA ATGGATGCTT TTTTTTGTGG AAAGCTTTCG CAAACATGGA AATAAAAATA 240 TCTTCTTCTC GGTTAACAGG ACTAAAGGAT GTAAACATAA ACCAGATGCC AATCCTTGTT 300 TCTCTACAAT CCCCTTCTCC CTCATGGCTC TGGACAGGCT TCTATTGTAA AACTATTTCT 360 ATGGCACAAG GAGACATATC AAATGAATGA ACATTGGTCT GCACGGAGCA ATACAGACCA 420 GGTTCAAAAG TCAAATGTTG AGTGAAAAGA GTAAGTTGTA GGATGTTCCA CATAGTAGGA 480 TATCATCCAG TAAATTTGCA AAACACTTTA TTCCATGTTG TCATGTGTAA TACAACAAAA 540 ACCTTGCATG GGGAGTATCT CGGTGACCTT TAGGGAGCAG GCTACCTTGG GGAAGCAGGG 600 CAGACAAAGA GTGCAACCAC AGGGCTGGGA ATTCAGCTGA ATCTGTCCTA TTTGAGTTCC 660 ATAGTAAGAG GGCTGACAGG AATACGACCA ACTGATAACA TTTCCTAAGT CTGGGTGAAA 720 AGTACCCAAA CAGCTACTAC TTGAGCTGAG CGTAGAAGCC AGGAAGGAAG AGGGCGGGGG 780 AAGACAGGAC CTTAGAATGA CGCCAGGAAG AATGGTGGAA GAGCTGACAG CATGGAGGAA 840 GAGCTGGGAA CAGCGCTTAG GGCCCACCTC CTGAGCCCAG GCTTGGGGAG TTACAGCAGT 900 GCTGTCCACA GGGGCTCATC AGAGTGGACC TGGTACTTGA CAAGACAGGA GTCAGCTTGC 960 TCACACACTG CTTCCTTTAC CATCAAAGTC TTATGTAAAA ATAAAAAATA AAAAATCAGT 1020 AGAACTAAGC AGCGTACTTT GTACCACAGC TGACTCCCAT TCCATGTAAG CTCCTGACCT 1080 TCTCACAGCC CAGCACTTTC GTGCATTAGA CAATGAACTG TGCTGGAGAA GATGATGCCT 1140 GTTCCCATGA GTCTCCCAGG TCTCCTGGGA CAGAAGTGAA GGGAAAGAAG GGTCCATGAA 1200 GAGACCTGGA GTGGAGTGGG AGCCCCAGGG GCCCAGTGGA TAGGGTGGGG TGGAAAAGGA 1260 CAGCATAGAT GGGCAGAGCA CCTCACGCTG CCTTCTGGGG CCCAGGGAAC ATCTAAGAGT 1320 GTGACGGGGC CTGGAAAGAA AGCCGAGCCT GGCCGGGCGT GGGGGCTCTC ACCTGTAATC 1380 CCAGCACTCT GGGAGGCCGA GACGGGTGGA TCACCTAAGG TCAGGAGTTT GAGGCCAACA 1440 TGGTGAAACT CCGTCTCTAC 1460
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