Tag | Content |
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EnhancerAtlas ID | HS092-02634 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:95222940-95223970 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr1:95223014-95223032 | CGAAAGGGAAAGGAAACC | + | 6.09 |
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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 |
GH01I094757 | chr1 | 95223060 | 95224338 |
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Enhancer Sequence | ACACTTATTA TGGGCAATTT TCTAAACCAT TCTATGTATA TTAAGGCATG TTAAAGAGCT 60 AATTATTTAG ATAACGAAAG GGAAAGGAAA CCCCTCCTTC CCAAGAAGCA GCATGGCACC 120 ATGCATTATT TGGTGTCACC TGTCAGCAAA CCACAATGTG ACTCTAGTCT CCGGTGTGGA 180 TGCAGGTCTC GGGGCTGAGG CTCTGCCTGC AGTTGTGCCC CATTATTTGT TTGGAAATGT 240 CACAAATAGG AATGCTTCCA TGAGAACCCT GACACCAGGA ACTTAAAGGA ACTGCTTACT 300 TGCACAGGAA CAGCTCTAGG CAGAAACCTG AGTTAACTGA CACTGCGTTT CCAGTTTATT 360 CCAGTGTGGT TTTAGTGCTC CTTCAAAACT AGTATCCCAA GCAGTGTCCA TAAGCCCCAG 420 AGACTCCCTC TTTAATTTGC CTGGGTCTGC TGGCCTGAGA AAAGTAACCG GGCTTTGTCA 480 CCAGTCTTTT CCTCAAAGAC CTTTTCTGAA ATCATCTGTG GTTGGGGAGG CTGAGGTTAA 540 TGGCAGTCTG GTCCCCAGAA AAGTGGGGCT GCTGTCTTTG GAGAGTGTTG CTTCCATATG 600 ACATTAAGTG CTCCTTTGAG AGTTCAAGGT TAACTTCCAG ACAAAACAAA CAAGGCTTTC 660 TGCCTTGTTT GCATCTGCAC AAGCTGGGAC ATTGTCTTGG CAGGAAGACT CAACGGTTTA 720 GGGAAGGACA ACAGGCAGAG GAAAGCTGAT CAGCCTAATG GTAAGATTGG CCCTGCTCTG 780 TCTCCCAGTG GCTCTCTGTT TATCTTGGAC TCGCTTAGCA ACGTCCAACA GGCTGGACGG 840 AGCCATTCCC TGGAGGGTTC CTTGAGCCTA CGCATCTCAC AAGCCTCCCC CAGAGGGATT 900 CCGCAGTTCC AAGAAGGGCA ATGGCGTTTG AGGGGGCAGC TGGGTTACTC TTCAATGAAC 960 TAAACGACTC CTTTAGAAAC TACAGACCAA ATAGTATGAG GGTGCCTGAA AAGAGGAGTA 1020 ATAAACAACA 1030
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