Tag | Content |
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EnhancerAtlas ID | HS073-02182 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr11:9385320-9386510 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr11:9385932-9385947 | CGCTGAGTCATGGTG | - | 6.43 | TCF7L2 | MA0523.1 | chr11:9386372-9386386 | GAAGATCAAAGGCA | + | 7.31 |
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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 |
GH11I009361 | chr11 | 9382592 | 9387533 |
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Enhancer Sequence | CTTGAACCCA GGAGGAACCC AGGAGGGGGA GGTTGCGGTG AGCCGAGATC GCGCCAGCCT 60 CGTGACAGAG GGAGACTCCG TCTCAAAAAA AAAAAAAAAA AAAAAAAGGA AAGAAAGAGA 120 AAATACAAAC AAAAGCTGAG ATTTGCTGAG TTCCTACCAT GTGCTACGCA ATGCCAACAA 180 CAAGGTGGCA TGGAATAATC CTCATGTCTG TTAAGTGGGT GGGGGTAGGA GTGGGGGTAG 240 GAGTAGGGGA GTGTCACACA TCTGCAAACG GTAACGTTGA ACTTCCAAAG TAGGTCCATC 300 GGGCTCTCAG GACCCGCGGC TGTCCGAGGC CTCAGTTGCC TCAATTAGTC TTAGGCTAAC 360 TTCCTCCTTG CGCTGGGGGG TGGGGAATAC TTTCCCGTGC GGAGGCCTCA GCTCCTCAAT 420 GTACAGAGAA GAGCCTTGCA GGGCCTAAAC ACTGGAGTTC AGGGATCCTT TATCAAGCTG 480 CCAAACCTTT TCAGGGGCTT GGAAGGACAC CTAAGGGCGG AAGCGGGCGC GTTGTGGCCC 540 CCGTGGGGCA GTGGGAAGGC AGCAGGGCCT CGCGGGCGGA GGCCGGAGCG CCGCTGACGC 600 CGGAGCGGAA GCCGCTGAGT CATGGTGGGG GCAGGAATGC AGCGCATTTG GAGAAGGCCC 660 GGGACGCCGG CGGCTCCAGC ATTACTGAGC AGTGACTTGG CGTCCGCACC TTCACTGCAG 720 TCGGGAACCA CCAGTGACGG CGGTGACCGG AAGAGCTGAG TCACCGCAGG CGACGGCGAG 780 CGACGCCGGC GGGGAGGGGC TGACGCGCCT GGGGCCGCGC GCCTGGGCTC CAGGGCCCCG 840 CGCGTCGCCA CGATCCCGAC GTTGCAATCC CCGCCAGCTC GGCGGGGGCC GCACGGGGCT 900 GGGTCTCCCG GATCCCGCCC GGGGATTGGA GTCTGAGGCT GAAATTTGAA ATCTTGAAGT 960 GGCCCCAAGC CACAAATACT ACAGACTGGT TTCAGTGGGA ATTAGGACCT TGTGAAAGGA 1020 GACAGCAGTG CCCCAAAGAC TGGGTAGATT TTGAAGATCA AAGGCACTTG CCTAGGAACA 1080 AAAATGATTT GCCTGACTCA GTTCCAAAAT GCAGCAAATA ATAATTAAAG CGAAACACAC 1140 ACGCACTGTT TTTTTTAAAT GCAAGAGCAA AACTTTTAAA ATTCCAAAAG 1190
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