Tag | Content |
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EnhancerAtlas ID | HS073-02646 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr11:75879900-75881070 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr11:75880159-75880170 | GGCCAATCAGA | + | 6.02 | Nfe2l2 | MA0150.2 | chr11:75880709-75880724 | TGCTGACTCACAGTG | - | 6.34 | RARA(var.2) | MA0730.1 | chr11:75880467-75880484 | TGACCTTTGACTGCCCT | - | 6.53 | TFAP2A | MA0003.3 | chr11:75880895-75880906 | TGCCTCAGGCA | + | 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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Enhancer Sequence | TCTGGGGAGG GAGTGGCATT TAATCCAAAC TCAGGAGATC ACTAACACTC AGAATCTTGG 60 AAACTCTGTG CCTGGAAGGA CTCTTGCTGG TCACTGAAAC CACCCACCCC ACTCAGCAGT 120 AGCCTCCAGC CCTTGCTTGG ACACTCCCAG GGATCGGAAG CGCACTTCTT CCCACTTGGG 180 TCAGCGCCTG CCCTTGTGGG ACTGCTGTGA CTGGAGGAAC ACCTTTTCTC CCACAGAGCC 240 AAGAGCTGTG TGCCTCCCAG GCCAATCAGA GTCTGGAGGC CACCACAGAG GGCCCCTGGG 300 TCCTCTTCCT TCCAGGCAGG CAACAAGGGA GGAATGGGGT GAGGTGGACC TCTGGGGCTG 360 GGCTGGAGAG GGGGGAGGTT CCCAGCTCAG GCCACAAGGG CAGAGCAGGA AGTTCAACCC 420 CACCTGCCAC TGATGTGTGG CCCCCACGAA GTCTCTGCCC ATCTCCGAGT CCTATTTCTC 480 CATCTGGAAA TGAGAGAGGG CAGCTGAGAG GCTGACAAGC TCCCAGTTCG CAGTGTGGGC 540 ATCATCAAGG GCTGTGGGAA TCTCAGGTGA CCTTTGACTG CCCTCATCTC CCCAAGGTTG 600 TGGGGGTGCC GCACCAGCAG CTCCTTCCAA GCATTGATTC ACAGCTGGGG AGCACCTGGT 660 GGGCAGATGT GGGCTCCCGT CACCCTGCTG GATCCTGCTT GTGTGCAGGC ATGAGTGTTC 720 GTGTGTGTGC GTGTTGTGCA CATACGTGTC TGAGAGTGCA TTGGGAAGTG AGGGCAGCAC 780 CCAGTGGGGT CAGGGGAAGG TGCTGGGTCT GCTGACTCAC AGTGGGACCC TGGGAAGTCC 840 CTGGCCCATC GCGCCCAGCC CCTCACGGGC CCTGAGTAGT GCCCTTCTGA GCAGAGCCTC 900 CGCTGCAGCT CAGGGCCCTG GGGCTGTGGG GGCGTGAATG TGCCTTCTCC GCCCCAACCT 960 CCGCCCGTGC CAGACACCGA GGCAGCGAGT GAGTCTGCCT CAGGCAACGA GTGTCTCAGG 1020 AGGATGCAGC CATGCAGGGC ATTTTCTGAG AGCAAAGAGA GCCTGGTGTC AAGGTTGGGT 1080 GGAGGGGGTG AGGCCTTGCT CCACCTCCCA GAGTCTGGTT GGAGGTGCAG GGAGAGGGGT 1140 CACTGGCTCC CCCAGAGTCG GCCCCCAGAG 1170
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