Tag | Content |
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EnhancerAtlas ID | HS038-22576 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr9:107730140-107731780 |
Target genes | |
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 | GCGCCTGTAA TACCAGCTAC TTGGGAGGCT GAAGCAGGAG ACTCTCTTGA GCCTGGGAGG 60 CAGAGGTTGC GGTGAGCCGA GATCGCGCCA CTGCACTCCA GCCTGGGCAA CAGGGTGAGA 120 CTACGTCTCA AAAAAAAAAA AAAAAAAAAA AAAAAAGAAG AAGAAATTTA ACATACAGGC 180 GATTTTTCAG GTTCTCATTT GCTAAACCAA CAATGCAGAA TTTGTGAAGT AGGGGCAACA 240 AGTTGCTGAA CCTGAGAGAC GCCTCTAAAT GCGCTCAGAG GTTATTTCAA CTGTGCTGTT 300 TGCTAGTTCA GGTACAACAG GCAAGACAGA AAGATGCCAC CGCTCTCTCC ACCCTCCCAG 360 CGCCGGATCA CAGAGCGCAG ACCATGCACC CAGCCTTCCA CACACGTCGC GATCTCGCCG 420 CTTTAAGCTG CTGGGTACCC TCGGCCCGCC CACAAGAAGG CGGGGCGGCG CGGGGTCTGC 480 TGGGAGTTGT AGTTTCGGGC CGGGCCCGAG AGCTTCTTGA CTCGTTTCCT TCTACCCCCA 540 CCGCCGCACA GCTGCCTATG GACTCTGGAG TTGCTGTGTA TTGAGCATGG GGCACAGCCG 600 GGGGTAAAAG GGGAGAAGGC TCCTTTAATC TGCGGATCGG GGCGCCGTTG ATGAGTGTTA 660 GAGGTGTTGG AACGCAGAGT AAGCGGCGCG CATGCGCGGC TGCCGGAGGT GGGGGCCGCT 720 CCTCCCGTGC CACTCAGGGG CTGGCTGCTG CCTTAGGGCT GACTGGGCTC ATAGGTAGGG 780 CCTGCGGTGC AAGTTTGTGA TAACACTGCC TGTAGGCTGC GGTTGTTAAG GCAGAGATTT 840 GAAGGGGGTC GGTTGGGGGT GCTGGGTAGT GTCAGTAATC AAGGGTTTTA ATCGCTACTC 900 CATCCTGGCT TTCGGGAACC TCCCACCTCC TACCCTTTCC CAGTTTGCAG AATTGCAGCT 960 TTCCCCATCC CCCACCCCGA TCGCTTCGTG GGAAGCCTTT CCATACTGTG TTGTGAAATC 1020 CGTTAGACCT CAGCCAAGGC CTTTTAGCCC GCCCGGAATT CAAGCTGCCC CCTCCTTGCC 1080 AAATCCAGAT CATGCGAGAC AACAAAAGGC TTGAGGCACA AGCCCTACAA GGCAGTGCCC 1140 CTGCCAGTTC TCCTAAACTT ATTGTTTACC CTGCCCTCTT CTTCCCCTGC AAATTCAGAC 1200 AGCCAGGCGA TAGATTAGAT AAATAGATTC CATGTCCTTA CATTTGCAAC AGGCTTTCAT 1260 AGATTCCTTT GCTCTGGAAG GTGGCATCAT TATACAAAAG GACAAGTGAG AACACACGAA 1320 TGTAATCAGT GGCAGAACCC TGGGACTGAA CCCTACAGGA GTTCTAAGTC TATTGTTTCT 1380 CCTACCACTT CACAAATGTG TCAGAAAGAG CTGAATGAGG TGACCAGCTG CACCTGACGC 1440 TAGCTGGCTT TCGGAATGCT CAGGCCCTGG GCCCTTGGCT CACCACAACC ACTCTTAAAT 1500 TGACTAACAA TTGCCCCTTA GTGAGTGACC TCTCCAGCAA GCCCGGAGGA TTTTGCCCAG 1560 GGTAATGTTT CACATTGAGC ACATACTTTG TGCTGGGCCC TGGAAAGGAT GTACATCAGA 1620 TCTTAAGTTA AAAGTTTCCT 1640
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