Tag | Content |
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EnhancerAtlas ID | HS003-34692 | Organism | Homo sapiens | Tissue/cell | A549 | Coordinate | chr4:40662650-40664440 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr4:40664286-40664298 | GTTTGTTTGTTT | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATAACTGTCC TATCTCTAAC ACACACAGCA TGTTATTTCT ATTTAAGAAA GGAAATGGAA 60 GATGTGAGTT TTTGTCACAA TCACTTTTTC TCAAATCTGG AGAGTTACCT GTTTTCAAAG 120 GCACCTTAGG AAGCCTAGGA GAAGCCCATG ATCATTCCTT TTTTTTTTTT TTTTGAGACA 180 GAGTCTCTGT CACGCAGGCT GGAGTGTAGT GGCGCCATCT CAGCTCGCTG CAACCTCTGC 240 CTTCTGCATT CAAGCGATTC TCCTGCCTTA GCCTCCAAGT AGCCAGGATT ACAGATGCAC 300 TACCACACCC AGATAATTTT TTGCATTTTT AGTAGAGACA GGGTTTCGCC ATGTTAGGCA 360 GGCTGGTCTT GAACACCTGA CTTCAGGTCA TTCACTCCCC TCGGCCTCCC AAAGTGCTGG 420 GATTACAGGC ATGAGCTACC GCATCTGGCC TCTTTTTTTT TTTTTTTTTT AAGACAGGGT 480 CTCACTCTGT GGCCCAGGCT GGAGTGCAGT GGTGTGATCA TAGCTCACTG CTGGGACCAC 540 AGGTATGTAC CGCTACATCT GGCTAATTCT TTTTTATTTT TTTGTAGAGA CAATCTTTTT 600 TATTTTTTTG TAGAGACAGT CTTTTTTATT TTTTTGTGCA TTCATTCTTG ATCACTCAAC 660 TCATTTAACC AAGTGGTTCA ATTCTTCAGA ACGTTCCTTT TTCCACAGAT AAACTAGGAA 720 TAAAAACAAT GAACCAACCA CAGAAGTTCA CCTTTTTCAA TCTTGATGCC ACCACAGGAA 780 CTGGAAGACC TATGTTTGAC CACCACCCCC ACTCCCCAAC CCTTGACTCC TGCCAACCCC 840 CGCCTCACTT ACAAACTATA TGATTATAGC AGCTGTGAGC AGGAGCAATT TGCCCAGACA 900 GACGGAATTT CCATCTTGAC TTAACTTCTT TCTAGAAGTG GAATCAGAAA ATACTGTGTA 960 GTCATCTGTG TCTCAGTTTC CTCATCTGCA ACATGAGAAT ACAAATAATA GCACCTACCC 1020 ATATGATTTT TATGAGGTTC AAATGAGATG TTACGTAAGG CATCTAGCAC AGTAACTGGC 1080 GTATATAGTA CAAGTTTAAC CAGTGTCAAC TATCATCATC ATCATCATCA CCACCACTAT 1140 CATTATATGA CTCTTCTGAG ACTTACTTTC CTCCCTTGTA AAATCACAGG TAGCCTACAG 1200 TCTCCATAAC CAGGAACGGG AGTGGTCTTC TCTCTGTTTT GCTAATGAGT AAAATGAGGC 1260 AAGGCATGCT AAAATGACAA TTCTCACAGA ATGAGAAAAG AGAACCCCTG AAGAGAATGG 1320 TGAGCTCCAT TTTGAAGCAA TGGGTCTGCT GTGTTCTTCC TGGCCCCAGA CCACACAGGA 1380 CTCCTGCCTC AGGGTTCACA TCAGCAGGGC ACCTTGAACC TGCTCTGACG GGCTCCGGAG 1440 AGCCAACTGT TAAATTTTCA GAAAGTCTGT AAGCCAGTTG TTAAACACAG CCATTACTAA 1500 AATTAAATTA TATGAACTTA CGATGAAATA CATTACACTT ACAATGGAGC AATACATACT 1560 CAAAACTTAT CACTTCCTAA TGATTTTATT ACAGTTCACT GTGGTTTATG TTTTTAAGGT 1620 TATTTACATC AATTGTGTTT GTTTGTTTTT GAGACGGAGT CTCGCTCTGT TGCCCAGGCT 1680 GGAGTGCGGT GGCATGATCT CAGCTCACTA CAACCTCCAC CTCCCAGGTT CAAGCAATCC 1740 TCCTGCCTCA GTCCCCACTA GTAGCTGGGA TTACAGGCAT GTGCCACCAT 1790
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