Tag | Content |
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EnhancerAtlas ID | HS182-09449 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr17:41658110-41659570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr17:41658980-41658991 | GGAGGGTGTGG | - | 6.32 | TCF7L2 | MA0523.1 | chr17:41659308-41659322 | CTCCTTTGATCTCT | - | 6.31 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 41658967 | 41659536 | chr17 | 41658886 | 41659366 |
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| Number: 2 | ID | Chromosome | Start | End |
GH17I043581 | chr17 | 41658472 | 41658623 | GH17I043582 | chr17 | 41658650 | 41659550 |
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Enhancer Sequence | CCAGAAGACA GAGGTCGCAG TGAGCTGAGA TCTGGAGCGC CACTGCACTC CAGCCTGAGT 60 GACAGAGCAA GACTCCATCT CCAAAAAAAA AAAAAAAAAA AAAAGACTCT AGGCATTTTT 120 TGTATTCACA GCAGTAAAAT CTCTGATTGC AGCTCTGATT TGAGCAAGAA GTAGGGATCA 180 TTGGCTAGTG TAGGGCTGGG AAGAGCAGAG GGGCAGTGGG AAAGGATGTA TATTTGGGGA 240 CGATTTGAGG GGTAGAAGGT TCTCCAGGTG GGAGGCGACA TGGTGTTTGA GTTGTGAGTG 300 GAATAAATGT CCCGGGGTCC CCTGGTTCAC TGGTCCCAGC TTTGTCTCTT CCTATTTGCT 360 TATCTGTCTT TTCACGTGTA TCTATTTGGT GCATCACAGT TGGTCCTGCT TTTGCTTGCA 420 TTCCTGGTAA ACTGGAATAA TTAGAGTTAA ATTTTCAATT AGAATGTTAG CGGATGTTCT 480 GTTAATAATA ACAGTGGCGA ACATTCCACC TCACTTTAAG CTTCCTGTGG AGCTAGGTCC 540 TTGGAGTCCA GAAGGGCTGG AGGAGAAAGA AGCCGGAATA CAGGAGGGGT GATGGGTCAG 600 CTAAGGTCCC CACTCTTTGG CCTCCTCCAC AGACTGGCTC CCTTTGTGGT TTGCACGTCT 660 CTGAACAATG TCTGCTGATG TTGTCTTCCA CACACACTGG CTTCTAATTC TCTCTCTCTG 720 TTGCTTAGGC TAGTCTTGAG CTCCTGGGAC CAAGGGATCC TCCTGCCTTG CCCTCCCAAA 780 AGTGTTGAGG TTACAGGCGT GAGCCACTGC TCCTGACCCT GGTTTCTAAT TATAATTGCC 840 TCAAAAGGTT GGCAGGCTGG TGGGGCTACG GGAGGGTGTG GGAGGTATAG CACTTGGAAT 900 CTGGTTTTGG AATTCTTCCT ATTTTTGAAA ATATAGCCAG TGACATCTGG GAGAGTCCAG 960 CTGAAGGCTG GAGGGCAGGG AGAGGGGACT GAAGACCTTT CCACTGTGCT GGGGACAGGA 1020 CACCCTGCTG GGTGGGCCTG CGGTCCAAGG TCCAGGACAC TCCCTCGGGC TTACATCCAA 1080 GGTCTCCCCA GGCCTGGCAC TTACTGGAGG AGGCGGGCTC CTAAAGGCCA GCACGCAGTC 1140 AGCACACCAG GAGGGCACTG AGCATGGGCA TCTCCTGAGC CCTCTGGAGA GGAGGCAACT 1200 CCTTTGATCT CTGGGTGGAG GGAGCCATGA TGTGTGTAGT GGGGGCAATG GGCATTCACC 1260 ACCATCTTCT TCCTAATTCT CTGCTACAGA TTCTCTTCCT GATCTTCATG CAATAATCTC 1320 AAATGTCTAT AAGAGGTGAT CACTACCATA AGAACCCTTG AATAGTGGTT CAAAGCCTTG 1380 TCATTTCCCA TCCCTAGTTG TTCCCCCAAT TCAGACCATG TCATCAGGCA GTTGGCTTAG 1440 AAAGAAACAT TTATTTATTT 1460
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