Tag | Content |
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EnhancerAtlas ID | HS176-16442 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr17:41773200-41774770 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr17:41774026-41774038 | GCTATTTATAGC | - | 6.32 | MEF2B | MA0660.1 | chr17:41774026-41774038 | GCTATTTATAGC | - | 7.22 | POU4F2 | MA0683.1 | chr17:41774511-41774527 | GTGCATAATAAATGTG | + | 6.77 |
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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 | GCCCAGAGTG TCTGGGGACA GAGTGGTAAA TTCTAATCAA GCCTTCCCAT GGCTTTGTGG 60 ATGAGGATGA GTTTCTACCC TGAAGCTCGG CCTGTTCAGC CATAAAATCA GGATAATGGT 120 GGCTGTGCCT CCTTAGAGTA GAATGAGAAT CAGAGCAGAA CAAGGGAAAG CTGCAGTGAC 180 TTGTCAGGTG TCAACCTTCA GCATGATGGG AGAGCCATGG GACCCTTCCC CTTTCCCTAA 240 GAGAGCCAGC CCTCACAGCA GGCCTGGGAT CCAATGCCCA GCACCCAGCT GGGAGCCCAG 300 GGACCTTGGC CAAAATCTGG TTCTGCTTCA ACTTGGTGCC CGGCCTTTGT CAAGTCACTT 360 CCTCATTTGC AAACTGGGAG AGTTTGGATG AAACTATTGA ATGAAATTAT TTTGGGGGTT 420 TCTTTCTGGC TCTCACAGTC CTCGCATGCT CACCATGTTC CCTTCAATTT CATTAGCACA 480 GCCCAACAAA GGGTTAAGCA GTGGCAGTTC CTCTCGTTCT TTGGTTAGGA CAGGAAGGTC 540 AGGGGTGAGG CCAATACAAG AGGTAGCCGC CACAGCTGAT GCTGGAAATG ACAATAGTTC 600 TTTCCTAGAC TCATATTTGT CCCCTCTCCC TGAAGCTTTG CCTGCAGTGC CCTTGTAAAG 660 AAGTTGGCAA GAAGCAGGAG TGAGGCTCAG CCCCTCTCTG AAATGGATAC GCCGGTTGCT 720 CCCCCTCATG GCTGGTCTCA TTTGCCTTCT TCATTTTTAG ACACATTCCA AACTTTTCAG 780 CAAATTATAG TGTTTGCCAA CTGGCCGTCT GGGGCCCAGG AGAGATGCTA TTTATAGCGA 840 TGCTGGGATG CTGCCATCCC AGAGCAGCCT GGTAAGAAAC GGAGCCAGAG TGCCTGGGAG 900 TGGCGTCCTG CACCCTGGGG AGAGGCCAGG GCCCTGGAGC AGGGTGGCAA AGCTGGTGGC 960 CCGTGGCAAG GACCACTGGC ACATCCCCTG CCTGCCTGGG CCCTGGGGTC TGTGCCCATA 1020 CCCCACACGG GGGGCTGCTT CCGTGCTCCT TGGAGAGACG ATGGTGCTGT GGGGCCACTG 1080 AGCACAGTAA AGGCTAAGAC CCACCATAGG TCAGCCCTTG CTCATGCTGA CTGTTGCCCC 1140 ATTTCCCTTC ATTCTCTCAC TCGTTCATTC CTCAGAATCT GCATCCTGGT TTTGTCACTA 1200 CCTGGAGTTG TAAAGATACC ACCAAGCTCA CCTTGTGGTG TGAGCCTTGA TTTTCCCCAT 1260 CTGTGTAAAG GGTGGATCTG AGCTCCAAAG TTCCTTCTAG TCATATGCAG AGTGCATAAT 1320 AAATGTGTTT GTATTCCCAC TGTGCTCAGT GGGCACTGGG GCATGCAGAA GAGAAATTGG 1380 AATAAATGTG ACCCTTGTCC TCCAGAGGCT CAGTACCAGA CTGGAACCAG GACCCAGATG 1440 AGGGGCCTAC CCAGAGAGGG CAGCGTGCTC TCCTATTTGT GTTAGGCGTT ACCATTTACA 1500 AAGGGCTTTA CGGCTTTGAA GGTCCCCACA ACGCCCTGAG GAGGTGAAGT GTGGCAATGC 1560 CCGTTCACTT 1570
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