Tag | Content |
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EnhancerAtlas ID | HS182-01918 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:221247510-221248580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr1:221247800-221247812 | TCCTGTTTACAT | - | 6.02 | Foxo1 | MA0480.1 | chr1:221247800-221247811 | TCCTGTTTACA | + | 6.62 |
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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 |
GH01I221074 | chr1 | 221247570 | 221248342 |
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Enhancer Sequence | GGGTGATGGT TTCGGGATGA AACTGTTTCA CCTCAGATCA TCAGGCATTA GATTCTCATA 60 AGGAGCACAC AACCTAGATC CTTTGCATAT GCAGTTCACA GTGGCATTTC TGCTTCTTTG 120 AGAATTTAAT GCTGCTGCTG ATCTGACAGG AGGTGGAGCT CAGGTGGTAA TGCTCACTTC 180 CCCGCCATTC ACCTGCTGCT GTGCAACCCT GTTCCTAATA GGCCACAGAC CAGTACATGT 240 CCACAGCCCA GGGGCATGGC AAGAGGAGAC ATTAGCAAAT ATGCAGATTG TCCTGTTTAC 300 ATGTCAGCTC TGAAGACTGT TGAGTTGATG GGTCTTCCCT TGGTTGCAAG CCAACAGCAG 360 TCAGAAGCAA GAAACCTTGT CTAGATTTCA CAATAACCTT GTCACAAGTC TCACGTTTCC 420 TGTAGGAAAG CTGAATTTAC CAGCACACTC ACTGTGAGTA AAACTGTAAC TCTGCTCTGA 480 GCAGAAGGCT TGTGCTGAGG ATAAAAACAA ATTCTCAGTG GAAATACAAA ATTGATCTAT 540 TAATTCCTGG ATGCTAAAGA CAATGATTTT TTCCTGTCTG GTGGCTGTTT TTCTTTTGTA 600 TGTAACTTTC AGTTTATTTC CGTAGTTAGG AAAGAGATAA AGCAACTTGA GAAAGCATAG 660 GAAGGTGTAG TCCCCTGAAA TCTAAATGAA GCCTGTTTGG TCTTGCAGTT TCCTGTGCAG 720 GTCTGGCCTG GGGCAGGACT ATATGGGCAT CTGCAGCCCA CACAATGTAG GAAAAAGACT 780 GGTAGAATAT TATCATTAAC TAAAGTAACT ATAGATGTTC ATTACTGAGC ACTTATTGTA 840 CAATGGCCAT TGGGCTAGGT GCTCTACCTA AATTACATTA AATTCTCACC ACTCTAAAAA 900 GTAGGTATCA TTTTTCTTTT ATGTGGAAGG GGCTGTGCCA CTGAATGGGT AAGAGCACAG 960 ACTCTGGCTT TCCACAATCT CGATTCATAC ATATTGGCCT TGTGACCTTG AGAAAGTTAC 1020 TTAGTCTCCT TGTGCGGCAT TTCTTTCATC TGTAAAATGG GGCTAAAACA 1070
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