Tag | Content |
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EnhancerAtlas ID | HS196-16268 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr2:191583260-191584330 |
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 | chr2:191584206-191584218 | ACTATAAATAGA | + | 6.22 | MEF2B | MA0660.1 | chr2:191584206-191584218 | ACTATAAATAGA | + | 6.37 | Stat6 | MA0520.1 | chr2:191583762-191583777 | ATTTCCCAGGAAAGG | - | 6.15 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I190717 | chr2 | 191582084 | 191584601 |
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Enhancer Sequence | GTCTTCAGGA CTTCCTGAGG CTGTGTCATG GGTGCATCCT CAACCTTGGC AAAATAAACT 60 TTCTAAATTA ACCGAGCCCT GTCTCAGACC TTCAGCGTTC ACAGACTATA CCGAATCGGG 120 CTGTTAATCT TTGAAAGTGA CTGGAACCCT AGAGATCTAA CCAAGATATT GTCAGGGAAC 180 TCAGCAGAGA GATCGTGAAC ATGGCAGAAC TGAAGGCAAG TGACTGTAGA AAAATAAATT 240 ATTTCACGCC TGTACTTCCT ACGAACAAGG ATTGTTTAGT AAACTAGATG TGGTAGCCAC 300 GATTTTCATG ATCAACAGAG TGGCAACAGG CAAGACTGAA TGATGGGGCT TTGGGGAATT 360 GCACTGGCGA TGAATCACCC TGAGATTATG CAGGTGGGGT TTCCCCTGAA GGGACTGGAA 420 CTGCTCACTG CCAGCTGTCC TCAGAAGAGG TCAGTCATGG GGCGGGAAAT CAGAATGCTG 480 GGACTAGAGT CAGTCTGACT GGATTTCCCA GGAAAGGTGA CTGTTGAGTC CCCAGGGCAC 540 TTCCTCCTGG AGGGGGAAGG ACCTGTGCCT GGCACTGACT TATTCTCTGT TTTCTGTTTC 600 CTTTCCATTG TCCCTGAACC TTTATTGTGA TCTGATCAGT GTCTCAAATA TTTTGACTTC 660 TGATGTCCTG AGAGGAATTA AGGGGAAAGG TCCACAACCA ACCCCTGAGG CAAAGCAGAG 720 GAGGGTTATG ACTTCTGTCC TCAGGCCACA GCAGTGGTGG CAGCCACAGG CACCAGCTGA 780 GAACAGCTTT GCCCCAGAGG GACCAGTTTC TGAATACACA TGACAGAGCA CCTTGAGAGA 840 GTCTCAAGAT TCTTTAGCAG AACAGGGGAC ACTGGGAGTA GGGGCAGAGG GCACTCATTT 900 TTGTCAATAA AACTAGTGTG AGTCAAACTA CGATGGCTTC AGTTACACTA TAAATAGAAT 960 TATCAAACAA GGGGACAAGC TCCTTGTCCC TACAAGTGCT TAAAAAATAA ATATTTTTCT 1020 TTTAAGGAGT TTTCTAATGG TGTTCCTATG ACATTAATTT ATTAAACATT 1070
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