Tag | Content |
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EnhancerAtlas ID | HS078-00388 | Organism | Homo sapiens | Tissue/cell | H2171 | Coordinate | chr1:18517180-18518920 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:18517503-18517521 | TCTTCCTTCTTCTCTTCC | - | 6.21 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGTGAAAGCC CCGGGCAGAA GGCTGGCCAC TTCTTTATCT CACAGGAGCC AGCCACTGGC 60 CAGCTGTTAT CGGGGATTTG TGAGCTTGTA AAACATGGCC AGCTATCACG CCATCTCCCC 120 AGGGCACAGT GCTTTCTCGG CTGGGCCTAA TCACCGGGTG ATCTTGGCCT GTGATTGAGG 180 GGAGAGCTGG GTTACCCTGG GAAGGCAGCA GCCAAGTCCT CTGGAAAAGG CTCGGGTGGG 240 TGGAGGAGCT GGGGGGCATC AGGGCCAGGC CTGCTGGGGC TGACACATCG CTGGAATGGA 300 CCATGGCAGA TTCCATGCCC CACTCTTCCT TCTTCTCTTC CCTGCAGGGA GATGGTAGAG 360 TGTGGGGGGA CCCTGCGAGG CTCCAGGGAC CCAGAAGGAG ATAATTCCAG AAAAAACATT 420 CAGAACTGCA TCAATGTCAG TGGCCCCCTC ACCCATTCCT CGTTAAGCAC CCACTCAGTG 480 CCAGGCCCTC TGCTAGGCTA TCCAAAGTGC TGGACTTTGC TGTGTGACCT CAGGCCAGTC 540 ACTTGCCCTC TCTGAGCCTC AAGTGTCCAA TAGGAATAAT AGTGCCCGTC TCACCAGGTT 600 ACTATGGGGA TCCCTTGAGG CAGTGGATAT GAAAGAATTG CCTTACAAAC TGTGAAGTCC 660 TGTGCCCATA AGGATGAGAT CAAAGGATAA GCCTGCATGT GGATTACACA CCTAGAGGAA 720 TGGCTTTAGA GGGATGAGGG ACATCTCAGG GGGACCAGAG AAGGACTCCC GGAGCAGGAG 780 ATTATGTGAG GCTTTGCTGA AGACTCTGGG GGAAGGAGGG GTTGAAATAG AGAGGGCATT 840 CCAGGCAAAG GGAATGGGAT CCATACGGTC TGCTGGGCAG GGGATACACG GGGTGTGTAT 900 CCCCTGGCGC GGGAGCACAC GGCTTGAGCT GTGTGGATCT GTGGCAGGCT TGCGGGTTGG 960 GGAAGCCGGG CCCATCTGGC TCTGTTTTTC TGCTGTCATT TTGGATGCTT TTGTGCTGAA 1020 TTCCCCTTTT GTCACTGTTT CCCTGCGATT TTCTTTTGAA CCTGGCATCT GTTTGGGGCT 1080 TCATCCGGTC CCTGCCCCCT GCGTTCTGAG GCTCAGATCT GTTTGCAACC TGGGCATCTG 1140 CTCTTAGGGC AGTAGGTGGT TCCGGCTGCC TCAGCAGGTC TCAGAGCCAG GGTCCGGGAT 1200 GGGTGGGGCA AGGGCAGATC TTTGTGGAAG GCGCTGGCCC TGCCTGACAC AAACATGTGA 1260 CATCTGCCCT CCTGAGAGTC CAGTAAGAAG CTTTCTTCCT CCCTCCAGCC CTCCTGGGCC 1320 GGGGAGGGCT GCCACGCTCT GTCATGCACA CCTGTCTCCC CCACCAGGCT TCAGATGGCA 1380 GAAGAGCCCA GCCTTCCCCA GCACTGGCTT TGGAGCCACG CAAGCCTGGG TGGACTCTTG 1440 GCGCTGCATT TACCACGTAA GCATCCTGAG CTAAACCTCC AGAAGCCTCT GTTTCCTGCC 1500 TCTGTGAAAT GGGGATCATG CTCCCACTTT GTAGTACCAT AAGGATGCAA CAAGATCAGT 1560 CTTGTCTAAC ACCTTCTTGC CTGTGGTCAG CAGACTGGGG CATGAACACG GCTCTGGGCC 1620 GGGTCTCTGG AGTCTGTATC TTGGTTCTTT CAAGGCATAT TAGTGAATCT CTCCCTGTGC 1680 CTCAGTTTTC TCATCTGCAA GATGGGAATA AGACCTGCTT CATAGAATTA ATGGAAGTAC 1740
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