Tag | Content |
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EnhancerAtlas ID | HS098-54169 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr8:21867300-21868500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NRF1 | MA0506.1 | chr8:21867847-21867858 | CGCGCAGGCGC | - | 6.14 | NRF1 | MA0506.1 | chr8:21867786-21867797 | GCGCCTGCGCA | + | 6.62 |
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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 |
GH08I022009 | chr8 | 21867112 | 21868911 |
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Enhancer Sequence | ATTTACATGC CCTTTGCTCG CCTACGCTTT TCTAGACCCC AAATCGGACC TAATCCTTCT 60 CAAGTCTCCC CTTACTGTGC CCATTCCTAA GAGCCTTAGG GCCCACCTAC TCTTCTGTTT 120 GGAGTGTTCC TAACCCCAAC CCCTGCCTGT CCCAGTAGCC AAAGTGTGCT TCTTACGAGC 180 TGGGCCCAGA CCATGGTGTC ATGACCAGCG ACAAGGATGT GCAGTTTCTG GGGAGTGTAC 240 AGTAAGGGGA GCGGTGGAAT TAATTTGGGT GAAGCCCCTG CAGAGAGACG CCAGACTGGT 300 TTATGCAGGT TAACCCTCAC ATCGCTGCCA TAGCTCGCTA CGACAATGAA AAGAGCAAAA 360 GCTATTGACA CCATCCCGCC TGCACCCTGC GAAAGAAAGG GAGAGTTTGC ACCCCACCTG 420 GCCTGACCTC CCCGACAGCG CTGCAGCCCC GGAAGTAATT TCGCGAGTTT CTTCCGCCGG 480 AAGGTGGCGC CTGCGCACTC AGGTGTCCAC GGCCTCTGTT CCGGCTCTCC CCCAGCTTTC 540 GCCGCCGCGC GCAGGCGCAG TCCAGACTCG GTCCTGGCCG GGGGTTCTAG TGTTGCCGCT 600 GGAAGAGCGA GGTCTTAATT GCTTTGCGGG AGCGTTCCTG GGGAAGTCCA GAGCTGGGTT 660 CCTGCGGCCC TTGGGCCCCC ACGGCGCCGT GTGCCTGGCA GAGGTTCGAG TTCACACGCA 720 CCGTGGCTTG CAGCAGGCAG CCGCAGTGCT AATCAGCGGC GCTGTTCCCG GGCTGGGTGC 780 AGCTGCTAAG GACAAGGCCC CTGCTCCGAA GAACGCGGTG GCTCGGGGAT ACCCTGAAAG 840 GGACGGCCAT GGCGCACATG GGATGCCCTA GGGTTCGTGG GAGGGCATGC AGGCGCAGCC 900 CCCGCAGGGG TTGGCCTGCC AGAGAAGGCA GGGGAGAGCA CTCGGGGCTG CACAAATGGT 960 GTGGCCGGAG GGAAGGTGCA GCCTTGTGTG TGTCTGGATG AGGGCTGGGC ATAGGAGCTT 1020 GGTATTTGAT CCTGAAAGCT CTGCGTTTCC AAAGGCCACT TGGCAAAGCA GCCTGGTGAC 1080 CAGTCTTTGT TTAGCCCACC AGCTAGTGGG GAATACGGAC TTGGACCAAG ACAAAGACTG 1140 CGGGGATAGT TGGGCGATGT TAGGAGAGGA GGGCTTTGTG ATCAGTTGCA TTTGGAGTAA 1200
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