Tag | Content |
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EnhancerAtlas ID | HS113-02766 | Organism | Homo sapiens | Tissue/cell | Keratinocyte | Coordinate | chr1:177875710-177877400 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chr1:177875905-177875919 | CCAAGATAAACAAT | + | 6.11 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGCCTCCCA ACCTCTATCC CAGCCTGGGT CCACCCTGTG AGATTCTGGG GCCCAGGAAA 60 CAGAGGATGT CATATAACAG GAGATTTTCA GAAGAAAACA ATTTTCAATG AGACGAATAT 120 GTCAGCAGAT TTCAATGGAA ATCCTGAATA AAGGACAAGG GCAACATTAT CCTAATGTTC 180 TTGCCCTAGG GCTTTCCAAG ATAAACAATC ATTTCCAGAT TCTCTACTCC TGGCCCTGCT 240 GCTGATTTGC TACTACTTTT CTTCCTTTTA TGGACTCAGT TTACCCAAAA TGCTGATCTC 300 TGAGCCCTGA GGTTGTATGA TTCTGTGCTG GACCAGCTCT CCAGGTATAG GTTCCAGCAT 360 CTCTCCAACA TGCTTAGCCT AGATCTAATG CTGATCACCA AGATGCTGTC ACCCAGGATC 420 ACTTTCTTTT TGATAAAGAG ATGTCCCTAC TCCAGTTCCA CTGGATCCTG GCACATCTGC 480 CAGGTCCTGT CCCTGACCAA AGTCATACAT CTTCCTGTGA GAACCCAGGT GGAGGAGAGC 540 ACATTCCCAT CTCAGCCCTG CAGGAGCACG GGAGTTCAAA GCCCGGGGAA GAGCTCCGCC 600 TAAGCTGGGT TCATGAATGC TTTATTATTG TTCTGCTGAA CAGTTACCCC CATGCCAGGC 660 AAGTCAGAAC AAGACTTCTA AGCTATGGTG ATGGATGTTT GCAGGGAACC CGTGGGAGTT 720 ATTAATATTC ATGTTCCCAT CACACTTTTG CAAGTAATGG AAGCTTGTTT TCTGTAACAC 780 ATCGTTAGGT GAGGAAGACA AGTGACCTCC TAGAGTTTTG AAGCACAAAG TGTGGTCACC 840 CAAGACCCAA AAGGGACTGA GGGAGGAGTA GACAAGGTGA GAGGGTTGAA GGTGTCATAT 900 TTTCTCCTTG TGGAGGCTCG CAAAAGATCC TTTCAACCCC TACAAAGTGA GCAGTTGTGG 960 AGCCTGGGAG CTGTTCACTG TCTCTCCCCT CTCACTGAGG ACAGCAGGAC TCAAAATGGG 1020 ATGTCTGAGA CCACAGGTTT GAGAGAGGGG AGTGGGGAAT TTGGATGCCT GAGTTGAGCC 1080 GTCTTGCCTA CCATAGAACA CTGGAGGGAC CTGCAGACCC AGGACCAAAA TGTCAAGTAG 1140 TCATGTGGGC CAGAGCAAGA GCTCACCCAC TGCCACTTTG AGCTTAGGGG AGACCAGATC 1200 CAGAGCAGCA AAGGATTGGA GGGAGGGAGG GTAAACATGT ACAGCAGCTA AAAGAGCCAG 1260 TCAATGGGGT GTGGGCAGGA CAGCAATGAT TTCAAACAGG CCTATTGAAG CTGCCATTTC 1320 CCCTCCCTGC TCTAAGGAAT AAAGTGCCCA GCCAAAACAG AAGCTGCTTT CACACACCCC 1380 AACACTGATC GCACTGTATT GCGTCTAGGT GTGTAGGCTT CCTGCCTCTG TGCGTGTTTC 1440 CTCATCCACA AAATGGGCAT AAGAGTAACA TCTCATTTTG TTGTGAAAGA GTTAATATAC 1500 ATAAACATGC TTAGAACAGC ACCTGGCATG CAGTACACCC CATTAAATGT GAGCTATCAT 1560 TACAACTACT ATGAGTATTA CATGTGTCTA TTTTCCTCCA TAGACTGAGT TCTCTAGAAG 1620 CAGGAACTGT GTCTTATTAT ATTTGGTACC CCAAAGCCCA GCACTGTGCC AGACACAATT 1680 TGGCTGCATA 1690
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