Tag | Content |
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EnhancerAtlas ID | HS127-32145 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr9:107730180-107731650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NRF1 | MA0506.1 | chr9:107730827-107730838 | GCGCATGCGCG | + | 6.02 | NRF1 | MA0506.1 | chr9:107730826-107730837 | CGCGCATGCGC | - | 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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| Number: 1 | ID | Chromosome | Start | End |
GH09I104967 | chr9 | 107730021 | 107731977 |
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Enhancer Sequence | ACTCTCTTGA GCCTGGGAGG CAGAGGTTGC GGTGAGCCGA GATCGCGCCA CTGCACTCCA 60 GCCTGGGCAA CAGGGTGAGA CTACGTCTCA AAAAAAAAAA AAAAAAAAAA AAAAAAGAAG 120 AAGAAATTTA ACATACAGGC GATTTTTCAG GTTCTCATTT GCTAAACCAA CAATGCAGAA 180 TTTGTGAAGT AGGGGCAACA AGTTGCTGAA CCTGAGAGAC GCCTCTAAAT GCGCTCAGAG 240 GTTATTTCAA CTGTGCTGTT TGCTAGTTCA GGTACAACAG GCAAGACAGA AAGATGCCAC 300 CGCTCTCTCC ACCCTCCCAG CGCCGGATCA CAGAGCGCAG ACCATGCACC CAGCCTTCCA 360 CACACGTCGC GATCTCGCCG CTTTAAGCTG CTGGGTACCC TCGGCCCGCC CACAAGAAGG 420 CGGGGCGGCG CGGGGTCTGC TGGGAGTTGT AGTTTCGGGC CGGGCCCGAG AGCTTCTTGA 480 CTCGTTTCCT TCTACCCCCA CCGCCGCACA GCTGCCTATG GACTCTGGAG TTGCTGTGTA 540 TTGAGCATGG GGCACAGCCG GGGGTAAAAG GGGAGAAGGC TCCTTTAATC TGCGGATCGG 600 GGCGCCGTTG ATGAGTGTTA GAGGTGTTGG AACGCAGAGT AAGCGGCGCG CATGCGCGGC 660 TGCCGGAGGT GGGGGCCGCT CCTCCCGTGC CACTCAGGGG CTGGCTGCTG CCTTAGGGCT 720 GACTGGGCTC ATAGGTAGGG CCTGCGGTGC AAGTTTGTGA TAACACTGCC TGTAGGCTGC 780 GGTTGTTAAG GCAGAGATTT GAAGGGGGTC GGTTGGGGGT GCTGGGTAGT GTCAGTAATC 840 AAGGGTTTTA ATCGCTACTC CATCCTGGCT TTCGGGAACC TCCCACCTCC TACCCTTTCC 900 CAGTTTGCAG AATTGCAGCT TTCCCCATCC CCCACCCCGA TCGCTTCGTG GGAAGCCTTT 960 CCATACTGTG TTGTGAAATC CGTTAGACCT CAGCCAAGGC CTTTTAGCCC GCCCGGAATT 1020 CAAGCTGCCC CCTCCTTGCC AAATCCAGAT CATGCGAGAC AACAAAAGGC TTGAGGCACA 1080 AGCCCTACAA GGCAGTGCCC CTGCCAGTTC TCCTAAACTT ATTGTTTACC CTGCCCTCTT 1140 CTTCCCCTGC AAATTCAGAC AGCCAGGCGA TAGATTAGAT AAATAGATTC CATGTCCTTA 1200 CATTTGCAAC AGGCTTTCAT AGATTCCTTT GCTCTGGAAG GTGGCATCAT TATACAAAAG 1260 GACAAGTGAG AACACACGAA TGTAATCAGT GGCAGAACCC TGGGACTGAA CCCTACAGGA 1320 GTTCTAAGTC TATTGTTTCT CCTACCACTT CACAAATGTG TCAGAAAGAG CTGAATGAGG 1380 TGACCAGCTG CACCTGACGC TAGCTGGCTT TCGGAATGCT CAGGCCCTGG GCCCTTGGCT 1440 CACCACAACC ACTCTTAAAT TGACTAACAA 1470
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