Tag | Content |
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EnhancerAtlas ID | HS068-02418 | Organism | Homo sapiens | Tissue/cell | GM18526 | Coordinate | chr17:37517380-37518890 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arid5a | MA0602.1 | chr17:37518183-37518197 | CTAATATTTAAAAA | + | 6.13 | MEF2A | MA0052.3 | chr17:37518746-37518758 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr17:37518746-37518758 | TCTATTTTTAGT | - | 6.32 | MEF2C | MA0497.1 | chr17:37518745-37518760 | TTCTATTTTTAGTAG | - | 6.57 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAAGTCACCT GAGTGTTAGG GAACAGGAGT TACAAGAATT AGACCATAAT GAAACCATGG 60 GAAGATCTAG AGAGGTGAAG GTCTAGAAGA AGGAGTTGGA GGATCAGAGA AGAGCCATCA 120 ATCAGAGAAG CCAAGCAGAT TGAGCTGCCA AGTTGATGCT GTGAATGGAG TTTGTGAAGT 180 CTATGGGAGG CCATTTCGCT GTTAGCTGAA TAGTTTGATA AACTAACTAT GATAAAGTAA 240 CATGAGAGAT ATGCAGAAGA AAGAACTGCA CAGTTTGCAA AGAACTGAGA ATATTGAGAG 300 CCTAGAATTT GCTGGATTGG AAAATAAAAC TTCCTCATCT TCTGTCTCTG GAGCCCAGAA 360 GCTTCTCAAA ACAAGAAGAA ATGTTTTTGG TCAGGCAGGG TGGCTTATGC CTGTAATCCC 420 AGCACTTTGG GAGGCTGAGG CAGGTAGATC ATTAAGTCAG GAGATCGAGA CCATCCTGGC 480 TAACACTGTG AAACCCTGTC TCTACTAAAA ATACAAAAAA TTAGCTGGGT GTGGTGGCAC 540 GCGCCTGTAG TCCCAGCTAC TCGGGAGGCT GAGGCAGGAG AACTGCTTGA ACCTGGGAGG 600 CGGAGTTTGC AGTGAGCCGA GATCGCACCA CTGCACTCCA GCCTTAGCGA CAGAGCGAGA 660 CTCCGTCTCA AAAAAAAATG CTTTCTTGGC CAGGCACAGT GGCTCATACC TGTAAATCCC 720 AGCACTTTAC AAGGCTGAGG TATGAGGACT GCCCGAGCCC CGGAGTTCAA GACCAGCCTG 780 GGCAAGATAG CAAGACCCCA TCTCTAATAT TTAAAAAGAG TAAAGTTTTA AAAATGCTTT 840 TGGATTTTGG AGCACTAAAA AAAAAAAAAA AATGCCCTGG CCAGGCATGG TGGCTGATAC 900 CTGTAATCCC AGCACTTTGG GAGGCCAAGG CGGGCAGATC ACGAGGTCAG GAGATCGAGA 960 CCATCCTGGC TAACACGGTG AAACCTCGTC TCTACTAAAA ATACACACAC AAAAAATTAG 1020 CCAGGAATGG TGGCGGGCGC CTGCAGTCCC AGCTACTCAG GAGGCTGAGG CAGGAGAATG 1080 GCGTGAACCC GGGAGGCAGA GCTTGCAGTG AGCCAAGACT GCCCCACTGC ATTGCAGCCT 1140 GGGCAACAGA GCGAGACTCC GTCTCAAAAA AAAAAGAAAA ATGCTTTCTT GGCCAGGCAC 1200 AGTGGCTCAT ACCTGTAATC CCAGCACTTT AGAAGGCTGA GGTACGAGGA CTGCCTAAGC 1260 CCAGGAGTTC GAGACCAGCC TGGGTAAGAT GGCAAGACCC CATCTCCTGC CTCAGCCTCC 1320 CGGGTAGCTG GGATTACAGG CATGTGCCAC CACACCCAGC TAATTTTCTA TTTTTAGTAG 1380 AGAGAGGTTT TCTCCATGTT GGTCAGGCTG GTCTCGAACT CCCGACCTCA GGTGATCCAC 1440 CTGCCTCGGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CCACCACACC CGGCTTTTTT 1500 TTTTTTTCTG 1510
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