Tag | Content |
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EnhancerAtlas ID | HS098-58070 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:107730330-107731820 |
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 | GTTCTCATTT GCTAAACCAA CAATGCAGAA TTTGTGAAGT AGGGGCAACA AGTTGCTGAA 60 CCTGAGAGAC GCCTCTAAAT GCGCTCAGAG GTTATTTCAA CTGTGCTGTT TGCTAGTTCA 120 GGTACAACAG GCAAGACAGA AAGATGCCAC CGCTCTCTCC ACCCTCCCAG CGCCGGATCA 180 CAGAGCGCAG ACCATGCACC CAGCCTTCCA CACACGTCGC GATCTCGCCG CTTTAAGCTG 240 CTGGGTACCC TCGGCCCGCC CACAAGAAGG CGGGGCGGCG CGGGGTCTGC TGGGAGTTGT 300 AGTTTCGGGC CGGGCCCGAG AGCTTCTTGA CTCGTTTCCT TCTACCCCCA CCGCCGCACA 360 GCTGCCTATG GACTCTGGAG TTGCTGTGTA TTGAGCATGG GGCACAGCCG GGGGTAAAAG 420 GGGAGAAGGC TCCTTTAATC TGCGGATCGG GGCGCCGTTG ATGAGTGTTA GAGGTGTTGG 480 AACGCAGAGT AAGCGGCGCG CATGCGCGGC TGCCGGAGGT GGGGGCCGCT CCTCCCGTGC 540 CACTCAGGGG CTGGCTGCTG CCTTAGGGCT GACTGGGCTC ATAGGTAGGG CCTGCGGTGC 600 AAGTTTGTGA TAACACTGCC TGTAGGCTGC GGTTGTTAAG GCAGAGATTT GAAGGGGGTC 660 GGTTGGGGGT GCTGGGTAGT GTCAGTAATC AAGGGTTTTA ATCGCTACTC CATCCTGGCT 720 TTCGGGAACC TCCCACCTCC TACCCTTTCC CAGTTTGCAG AATTGCAGCT TTCCCCATCC 780 CCCACCCCGA TCGCTTCGTG GGAAGCCTTT CCATACTGTG TTGTGAAATC CGTTAGACCT 840 CAGCCAAGGC CTTTTAGCCC GCCCGGAATT CAAGCTGCCC CCTCCTTGCC AAATCCAGAT 900 CATGCGAGAC AACAAAAGGC TTGAGGCACA AGCCCTACAA GGCAGTGCCC CTGCCAGTTC 960 TCCTAAACTT ATTGTTTACC CTGCCCTCTT CTTCCCCTGC AAATTCAGAC AGCCAGGCGA 1020 TAGATTAGAT AAATAGATTC CATGTCCTTA CATTTGCAAC AGGCTTTCAT AGATTCCTTT 1080 GCTCTGGAAG GTGGCATCAT TATACAAAAG GACAAGTGAG AACACACGAA TGTAATCAGT 1140 GGCAGAACCC TGGGACTGAA CCCTACAGGA GTTCTAAGTC TATTGTTTCT CCTACCACTT 1200 CACAAATGTG TCAGAAAGAG CTGAATGAGG TGACCAGCTG CACCTGACGC TAGCTGGCTT 1260 TCGGAATGCT CAGGCCCTGG GCCCTTGGCT CACCACAACC ACTCTTAAAT TGACTAACAA 1320 TTGCCCCTTA GTGAGTGACC TCTCCAGCAA GCCCGGAGGA TTTTGCCCAG GGTAATGTTT 1380 CACATTGAGC ACATACTTTG TGCTGGGCCC TGGAAAGGAT GTACATCAGA TCTTAAGTTA 1440 AAAGTTTCCT TTCCCCCAGG GAGACCAGGC TGTCCTATCA AGTATTCTGT 1490
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