Tag | Content |
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EnhancerAtlas ID | HS043-02284 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr1:110796910-110799300 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr1:110797078-110797088 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr1:110797078-110797088 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr1:110797078-110797088 | ATTTTCCATT | + | 6.02 | RFX2 | MA0600.2 | chr1:110798262-110798278 | GGTTGCCATGGAGACT | - | 6.06 | RFX2 | MA0600.2 | chr1:110798262-110798278 | GGTTGCCATGGAGACT | + | 6.28 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCTCTCTGCT CTAAGCCAAC CAGCCAGCCA CAGGATCTGA CCCCTGAGGC TTGGGAGGAT 60 GGTCAGGGTC ACTGTGGCAT CTTCATGTGA TTCAGTGCAT CATTTGCACC TCATGTTCCT 120 TCATTGCACC CACTGCATAT CCAAGAACAT CCCCAGAGAG TCATGGTCAT TTTCCATTTC 180 TCCATCTTGT GGCTTATCTG CCATGTGGAG GAGGCCAGGT TGGAGTTAAA GACTGGGGCT 240 GAGTGTGTGA CACCTGCTTT TTGAGAGCAG CCCTGGCATA GGCTGCTTGC TCTAAACTCT 300 GTACAGCTTC CTGCCCTGGG AAATGCAGAA TTAATTGAAT GACATGTGCA GTGATTACGG 360 GAACAAGGAG ATGAGTTGGG GGGAGGACTG TCTGTAGATC CTGCCAAGGA GACTAGGAAT 420 ATATTCAAAC CATCACCTTA TACTGAGCTC CCTCAGCAGG TGTCAGTGTA GCAGTCACCT 480 GGTCTATCCC AAATACAGCA CCTTACAGCC TGAGCACATA CTTTGCAGAG CCAGCCAGAG 540 CCTCTGGGAG GCCCACAAGA AGGCTGCAGC AGTGCTGTAG AACAGCCCAC AGCAGTTGTA 600 GCAATGCCAT TCCAGTCCAT TCCATTCCAT TCAATTCCGT ATTAGCTCAC CACCTACTAT 660 GTTCTGGAAA GGGTGCCAAC ATTATAAGTA AAATAATCTT CAAGTTGATG AAACTCACTG 720 CATAGCATAG GAGACATCCA AGTATATACA GATAGCATTT CTGGACTTGC AGAGATGATT 780 CTCATTTAAG ACATTTGGTA AACTCTGGTG AGAGCAGGGA ACATACACTC TCTTTTATTC 840 ACCCCTGTAA TCCCAGTGCC TGGCACAGAG CCTGGAGCAG AGTAGGTGCT TAATAGATGG 900 TTGGCAAATG AGCAAATGCC TAGATCGTCG GAGTTGGACA AACAAGTTCC CTAGAGCTCT 960 GCAGGGAGTT AAGATTCAAT GTGCTCTCTG TTGGCCGTCC CCCTGGAACC CCCTGGTTTC 1020 CTCTCAGGAG GTCCTCTTCA CTTCACCGTC TTCTCTCCAG CTCACCCCTT CACACTTAGG 1080 CTCTGCAGTT TTGCATTCAA CACCCTACTC CATGTCCCCA GGCACAAGTT GCCAAAGATA 1140 ACTAATATTA GCAGGTTAGA GTCAGCACAG ATATACTTTA AGATGCTTAG CGGGGCTGGA 1200 GAGTCCTAGA CAGAGCCGGG TGTATTTTTA GCTCTTTGGG TATCTGGAAA GGTATTGAGA 1260 TGCAGTCATT GCTACAGACA CCCAGGCAAA TCAGTATTCT GCTACTGGCC TCCCCATACC 1320 AGGCAGTTTC CATTCAGTGT CTCAAAAGCA AGGGTTGCCA TGGAGACTGA GTGCCAGGAC 1380 AACCGAACTT CCTCTCAGGA AACAACAGCA CAGGTGGAGC TCTGGGCCAA TGGGGATCAA 1440 GAAGCTTCTC AGATGGCCAC AGCTTTCTCT CCTGAAGGCA AACGATGGCA GAGGTCCCTG 1500 GCACCCTCAG AAGGGGTCAG CCAGAAGATG GAGGACACTG TCTCTGGAAC TTCATTCAGG 1560 GAGGGGTTGA TTCTATTTCT CACTCACACT TGCTGTGGAC TGCTTTAGTT CTCTTCCTGG 1620 CCCTTCCTTC CACAAAGGGA TTTGGCCACC CAAGAAGCAG TCTAGAAGCT GCTCAGGGAG 1680 GAAGGTGGCA GGGCCATTTT GCAGTAGAGG CTAGTTCTGG CAAACACCTA GAACACAAGC 1740 TCTGCAGGAG GCTGGGGGAG GCCATGTCAG TCCTGCAGCC ATTAGAATTA CAGTAGCCCA 1800 CTCTTCTGGG TGGCACTGTA CAGGACCATC TTATCCTATT CTTGCTATCA TCTGGGGAAG 1860 CAGCCAAGAC AGGTGGCATG ATCTCCACTT TCCTCCTGCA TTCGACAAAC ATTTCCTGTG 1920 TACCTGACAT GTTAGACAAG CGAGATGAAA ACCCAAGGCT CCAAGAGGCT ATGAAACCCA 1980 CCTACAGTTA CAAAGCTATT AAGGGTGGAA CCAGAAGAGC ACCCAGATCT CTCCAGTCCC 2040 TAGATTCAGA GGGATATGAG CCCAAAGAAT CTGTTAGAGA ATATTTACTG TGACCCTCAC 2100 ACTTCAGAGA AAATAAACTG AGGCCCCGAA AGAACACATA ACTTGGTCAC TCAGAACTTG 2160 TAGTGGAGCA AGGCCAAGAT TCTTTTGCCC AGTCTTCTCA TCACCCGTAG CTCTTCCCAG 2220 ATATTCCAGC TTTTACTGGA CATCACGCTG TGTCAGGCAG TGGATCAGCT AACAATTACA 2280 TTTAGTTGTG ATTAATGAAG ACCTGACCAC AATGACTTAA ACAGGGGCTT ACGTCTCACT 2340 CATAAAAGTC CAGAGGCGAC GGAGGCCTTG CTCGCTCCAG GCCCGGTCAC 2390
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