Tag | Content |
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EnhancerAtlas ID | HS127-26954 | Organism | Homo sapiens | Tissue/cell | Macrophage | Coordinate | chr6:45541500-45542920 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROD2 | MA0668.1 | chr6:45542080-45542090 | GCCATATGGT | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGTTTCTCCG CTGTTTCTCA CTATGAAACT CGTTCTTTTT TGTTTTGTTG TGCTGTGTTT 60 TGTTTGAGAC GGAGTCTTGC TCTGTTGCCA GGCTGGAGTG CAGTGGCGCG ATCTTGGCTC 120 ACTGCAAACC TCCGCCTCCC GGGTTCAAGC AATTCTCCTG CCTCAGCCTA CCGAGTAGCT 180 GGGATTACAG GCATGCATCA CCACGCCTGG CTAATTTTTT TGTATTTTTA GTAGAAATGG 240 GGTTTCACCA TATTGGCCAG GCTGGTCTCA AAGTCCTGAC CTTGTGATCT GCCCACCTCG 300 GCCTTGAAAC CCGTTCTTGC ACATGTTGGT AAATGTTTAA TAACTGGCTC TCTGAGAAAA 360 AAAAAAGGAA GAAAACAAAA GCCTTTTTAA TGGTGTTTAC TGATTTCTGT GATGTAAATA 420 TGGCAAAGTT CAAGCTATCA ATATGATGTC ACTAAAACCA GGATTGAGAA GTGATGCACC 480 ATTTTTTCTC ACAAGCTGGT GTGAAGAAGA CCTGGCAGTG ACAGATACTA AAATGACAGA 540 GGATTGTATG GGACAGTGTG GCAAGTCCCG CGGCTGAGAG GCCATATGGT CATGAAAGCA 600 CGGCTCTGTA GGTCACCACT GCTCTGTCTG GTGGCTCAGC TTCCTCGTCA ACCATGGTAG 660 TAGGAGCATG AGATGGTTGA GTTCTGAGGG GAAGTATGGA GGAAGAGGAA AGTCCCCTGA 720 GTTATTTTGT TTGCCAAGCA AAATATAAAT TAAGAAGCTT GCATGCAGCA TGGGCAGTTA 780 GCTGTAGATC CATTGGATGG AATTTTCTAC AACCTTAGGA TGGATAGAAG CTAATGACGG 840 TCTAGGTGTG CCCTCTATTC AATATTCTTT GACTGAAATT GAATTGATAT AGGAGCAGCG 900 TGTTGGTTTA GAATGAAATA GGACATTTCA TAAGCCAGCC AAAATGCAAA AAGCAGACAG 960 GAAAACCAAG CAGGACAGGA AAAACATCCC TTGAAACATG AGCCAGGGAG GGTTAGGTTT 1020 GAAATGACAA AAGATCTGAG CTCCAGAGAG TCCGAGTATT ACATTCTGAA CCAATTACTG 1080 ACAGAAGTCA TGAGGCTATG GACCTGGGGA AGGACAACCA TGGGTAATGG AAGCAGGTGG 1140 CTTAGAAAAA AAAAGCACCT TTCCTCTAGG CACACTCCTG GGTAATCTGG TGTGTTTGGA 1200 ACATGTATGA GCCTGAGACT GAGCTATCAG GACACAGGCC ATGGTGAGCC AGCTGGGGTG 1260 TGCCAGGTGC ATGTGGATCA TGCATTCCCC TATTGAGTTA CAACATCCTG TGGGTTCATA 1320 CCAGCCTCAC AGTGCTCCTT GCACAACCTG CTGTTCAGGG AGCTTTCCGT AAGGGCAGGT 1380 GCTTCCTCAC AATGAAGGGC ATGGACACCT GCTGCACTAT 1420
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