Tag | Content |
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EnhancerAtlas ID | HS002-09783 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr9:36316580-36318250 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr9:36316643-36316654 | TTTGTTTACAT | - | 6.14 |
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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 |
GH09I036316 | chr9 | 36316636 | 36321269 |
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Enhancer Sequence | TTAGAGCGAC TGCCAGATCT TATCATGCAA TGCATTAATA AAGTAGCCTT TATCTTGCCT 60 GAGTTTGTTT ACATTTTGAT AACTGTATTT CAATACAGCA GGTTCTGTCT GGAGTCCTTT 120 GTGCTTGTTT TAGGCATGAA GAACATGACT CCAAGAATCC GTCCATCCAC CTCCCCAGGC 180 TGCCGAAGAC GGGAGCACGG CACACAAGGG TGAGAACTGA GGAGGGCAGC TGGCAGGGGC 240 AGGCTCTGAA AGCACAGCTG TGTGAAGGTC CGGTTCAATA TCCGCTTCAG AAGACACACA 300 GCCCTTTGTT GCTCATGTCT GTTGCTGTCT AAAGTTGATC AAGGGCCAAC TTAGAGAACA 360 GGATGGAGCT GTGGAGAGGA ATGGGTAGAA TGCCATGGAG ATATTGAGAA CAAAAGGCCA 420 TGGCTAATAC TCCCACTCCG GCCCCAGCAC CCAGGCACAG GGAATCTGAG CCCCCTCCAC 480 CCACATCTGC GAGCCCCTGA CAGACTCAGC AGATGTCAGC TTTTTTGAAG AGACGGTGTC 540 TCTCTCTGTT GCCCAGGCTG GAGTGCAGTG GTGCAATCAC AGCTCAATGC AGCCTGGAAC 600 TCGGCTTTGC AAGTGATCCT CCCACCTCAG CCTCCTGAGT AGCTGGGACT ACAGGCATGC 660 ACCACCACGC AGAGCTCCGG TTTTTTGTTT TTTTTTTTTT GAGATGGAGT TTCCCTCTTG 720 TTGCCCAGGC TGGGGTGCAA TGGTGCCATC TCGGCTAACT GCAACCTCTG CTTTCCGGGT 780 TCAAGCAATT CTCCTGCCTC AGCCTGAGTA GCTGGGATTA CACGCATGTG CCACCATGGC 840 CAGCTTATTT TGTATTTTTA GTAGAGATGG GGTTTCTCCA TGTTGGTCAG GCTGGTCTCG 900 AACTCCTGAC CTCAGGTGAT CCACCCACCT GGGCCTCCCA AAGTGCTGGG ATTACAGGCG 960 TGAGCTACTG CGCCTGGCCT CGCAGAGCTA ATTTTTTACA GAGGCTGGGA TCTCACTGTG 1020 TTGCCTAGGC TGGTCTCAAA CTCCTGGCCT CAAGCGATCC TTTGGCCTAT AATCCCAAAG 1080 TGCTAGGATG ACAGGCGTGA GCCACCGTGT CCGGCCTCTG TCTGCCATCT AACTCGCAGC 1140 CTGCTTCTAT CATGTGCTGG AGAGCTGCCC TGCCTGCTGA AGAAAGCTGA GACCCCAAAC 1200 GTCTTTTCCT CAGGAAGGTG AAGGTGAACT TGGTGGCCTT TACCTGATGA CTCTGCTGAT 1260 ATTTGATCCC TGAGGGAATG AGCCACGGTT CAGCACCCAA CCCCCACTTG AACTCTGCAG 1320 TTTCCCAGTT TCATTAAGAA GCCCATTGTT GAGTCTGGCC ATGCGTCAAG GACACGTGGA 1380 CTCTTGGGGC AACCCCGTTT CTCCAGCATC CTCCCAGGTG ATGGGTTGGT GTGGCCAGGA 1440 GCCAACAGGA AGGGTGTGGG CCAGAGGGGA GAGGCTTCCT AGCAGCTGGC TGCCCTGGAG 1500 CTCCGGGAAG GTTTGACCAT CAGGTTTACT GCACCAGGAA TATATCCTTC AGTTTCCCCC 1560 AGCCAATCTG TAGAATAAGG AGAAATGGAG AGTGTAGGAA GATAACTGCA GTGTGGACAC 1620 AGCCTCAGGT TTCTTCTTCG GTAAAGCTGA TGTTTATTAC ACAGGGGCAT 1670
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