Tag | Content |
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EnhancerAtlas ID | HS031-00518 | Organism | Homo sapiens | Tissue/cell | Denditric_cell | Coordinate | chr1:43213990-43215440 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr1:43214189-43214200 | GCAGGGTGTGG | - | 6.62 | NFIC | MA0161.2 | chr1:43214173-43214184 | TTCTTGGCAGA | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGGCCAATG TCACACATGT TAGCAAGGGA GCACCTCGGG AGACGGCATA GCTCTCTTCT 60 TGGCAGGGGA GGTGCTTCCC AAAATGTGTT TGAGTCTACG GAATGCCCAA TGAACTAGGG 120 GGGTGTCTTT GGCTAAGCCA CAAGCCTAGG GGTCAGGACA AGTCTGCAGG CTTCCTAGGA 180 CAGTTCTTGG CAGAAGTGAG CAGGGTGTGG CAAGCAGGAA TGAAGGGCTC CAACCAAGGG 240 CAGATCCTGG GCAGAATGGC ACAACCCTGG TTTGTAGCTG GACTTTACAA AATACAAAGG 300 CCCAGGGAAG TGAGAATGAG GGATCAGGAG GTGGGACGGA CGCAGGGCAG AGTGGGTCAG 360 TCCTCCATCA GGACTGCAGG AGATGGGGCT GAGTGGCAGG AAGTGGGGCA GAGAAGAGCT 420 GGCTAGCAAA GGGAAAGCAT GAACTTCAGT GGGGCTCTGG GGTGGGGTGG GTGGAGAAAC 480 CATGCAGGGA GAAGGTCACG AAAGGGAACA GACCGGGCTC ACTGTCAAAT GCCAGGCAGA 540 CCACGTCTTT CCCCAACGCA AACCTTTGGC ATGCTCTATG TAGGCACCGT CACGTCGTGG 600 TGGGTGCCTC CTTCTCCATT CCCACTTGTC CAGCCAGTCA CCAGGTCCTG TCCATCCACC 660 TCCTGCACCT TCCCGGGGCC TCACTTCTCC CTCCTCCCAC TGCCACTTCC TGAGTTTAGG 720 GCTTTGCCCT TGTCCACAGA GGTCATTGCT GACCAGCTTC CCTTTTTGGT TTGAAATCTC 780 TCCACACACA CAGCAGCAAA ATGAATCCTT TAAAAGTCAA GGCCTCACCA CGTCCTTCAC 840 TGCTTGATGA GGCCTCCCTG GCCTCCTGGC ACCTGTGCTT GTGCTCTCCC ACCGGGGGCT 900 TGTGACACAC CCAGTTGTGT GTCTGACTGG TCCCTTTGGG TGTGCCCAGA TTGTGACAGA 960 ATTCCAAACA TTCTGAGGTA GAGGAAAGCC CTCTGATCTG TGCCACGTAC CAATGGCCAT 1020 CACTGCCAGG GGCCTGCTGG AGGCTCCAGT ATGACAGAGC CGGCTCTGGG CCACATAGGA 1080 TCCTTGCAGC ACTAGCTGAA CCTCTCCCCT TCTTGGACAT GCAAAAGGGA ATGTGGGTGG 1140 GCGAGGGAAT GAGGAATAAC CTCCAGGCCA CTCTCACTTG TAAATCACGA AGCTCTCTCA 1200 CAAATTTGGT ATTTAACAAT TAGTAAAAGA GAATCTGCCA CATAGCTATG GTTGAGCTAA 1260 AGGATAAAAA TTCCCTTGAA TGTAGCTCTC CAGGATTTGG CACCTTTCTT AGTTCCCCTG 1320 ACTACCAGGC TGCACAATGC CTCCACTCCT GTGCAAACAC CATCCCACCA CCCGGAGTAC 1380 TCCGTAATCG TATTCATCCT GCAAAACTGC CATTGCTTCC TCTGGGAAGC CTTCTTTTTG 1440 TTGTTGTTGT 1450
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