Tag | Content |
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EnhancerAtlas ID | HS044-09115 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr3:99158350-99160200 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr3:99160144-99160159 | AGTTAATGAATAACA | + | 6.23 | SOX10 | MA0442.2 | chr3:99158842-99158853 | TCCTTTGTTTT | - | 6.32 | SPI1 | MA0080.4 | chr3:99158598-99158612 | GAAATGCGGAAGTG | + | 6.48 | SPIB | MA0081.2 | chr3:99158600-99158612 | AATGCGGAAGTG | + | 7.22 | Sox3 | MA0514.1 | chr3:99158843-99158853 | CCTTTGTTTT | + | 6.02 |
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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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Enhancer Sequence | TCAACCAACT AAACTCCTCT GACTCTTCCT CCTACTTGTT CTTTCCTTCC ACTGATGTTC 60 CCTACATTCT AAATTTAGAA AGAGATACAT TTTTAAAATC ACTTATTTAT GAAAAAGGGA 120 GAGTTACATG AGATAGCTTT GGGTAGCTGA ACCCAAGGAA ACCTAGTTAC CCATTTTTGT 180 GAGTGTCCAC CCCAAAGGAC ATAAATTAAA CTAAGAGCAA ACTGTAGGAG TTGTCTCAGA 240 AGCTTTAGGA AATGCGGAAG TGACAGCAGG TAAAGATTCT CCTCTAAATC TCTGTTCCAA 300 AGGTCATAAT GGGAAAGAAA ATCAACATTT TTTAACAACA AACCTTTTTA TATGCTGTCT 360 TCCAAAGCTT AATATATATG TCTGGTGAAA CAAGGTCATT TGTGTCTGCT CTGCCCGTTG 420 TCTCAATTAT AGCTGTTTTA GGATTTGCTT CACAAAAGAG GTAAACAGGT TTTGGATCAG 480 AAAACAAAAA GCTCCTTTGT TTTCCAGGGA ATGGGATGCT GAGGTAATCC ACTACATTTG 540 TGGAACCTTC CCCAAGGGAG AAAATGGCAG GTTTTCCACC AAGAAATAAT TGCTTTTAGA 600 ATGATAAGAA AGGAAGTTAG TTACTCTTGC ATAAGTGCAT CTGTCCTGAC TGGCTGTAAT 660 TTTTGTTTTT AGTTTGCTCT TTTAGGTCAG ATGATATAAA TCATCATATT CAGACAGTTT 720 AATGTTGTTC AGCTACAGTT TGATTTTCTG GCATACTAAA TCTAAGTGTT AAAATAAATT 780 GGAGCCAAGT TTTACATTGA AACAAAGTCA TAAAACTCTA CATATTTGAA AATGAGGTGA 840 TTGCTTAACA GCTTGAAAAG ACTTAGTATT GACCTTGTCT ATTGTTTCTT ATAGAATAGT 900 ATTTACATTA ATGTCAAATT CCAAAAAGCA AAACTAAATG AGTCTAATAT GAACTACATA 960 TTAATTCATA CACACACACA CACACACACA CACACACACA GACACACACA CATACATAAA 1020 TTATTGTGCC TATGTCAGGA AAAGATAAAT ATACAGCCAG TTCTCATTAT TTGCTTTTGT 1080 GATCTTTTCT CTTTTGGTTT GTATTGTGTT TATTTAATCA AAGTCTACTT CTGATCCCAT 1140 TTCTCCCTGC ATTGTTTCTC TGAATCAGGC ACTTTGTTTT CCTTTCAAAT CCAGTCTTAA 1200 CTTTTTCTTC TTCCTTTTTC CTCTCTGTTT TCAGACTTCA TCTTATTTTT GTTCCCAGCC 1260 AATCTTTCAA AAATGTATTG AGCATCAAGT CTGCACACTA ACATATACAT GATTATATAC 1320 AGATGTGTAT ATGTGCATAC ACAAAGACAC AGAGAATCTT CAACTTGTGA GAACTCAGCT 1380 TCTAAATTTC AAAACTTCTA CCAAGCCCTT TGCATAATAT ACAAGACTCT TCATGATCTG 1440 GCATCTGCCT ACTTATCCAC TCTCTTCTCC ACCCCTTTCC CCCTTCATAC TTCACACTAT 1500 AGAAATACTG AGCTGCTTGT AACACCTCTC CTCTGCTTGC CTTTGAACAT GATCCTCACC 1560 TTAGCTAGAA CAAACCTAAA TCCTCTTCTC ATGGGTCATA GCCTTATCAT CCTTCAAGTC 1620 TGAGTTGAAT AGCCACCTCC TCTGAGAAGC CTTCCATAAG CACTCCCTAG GGGCTCATAA 1680 ACTCTTTCAC CCAGGCTATA ACCTCTATGA AGGCAGTAAC AATGTACAGA CAGACCAGGA 1740 TTGTTATATC TTTGTCCCTT CAATTCCTAG AATAATTCCT AACATGTAAT AGATAGTTAA 1800 TGAATAACAG ATTAGTGAAC CATCAAGGGA ATATACCTCT TGTGCAAAAG 1850
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