Tag | Content |
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EnhancerAtlas ID | HS188-06948 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chr2:26138540-26139930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYB | MA0502.1 | chr2:26139220-26139235 | AAACGCACCAATCAG | + | 6.73 | RUNX1 | MA0002.2 | chr2:26139582-26139593 | AAACCACAAAC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 26139400 | 26139546 | chr2 | 26139223 | 26139382 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I025916 | chr2 | 26139241 | 26139779 |
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Enhancer Sequence | CTCACCGGGC CTTAGCTGCC TTCCCGCCGG GCAGGGCTCG GGACCTGCAG CCCACCATGC 60 CTGAGCCTCC CCGCCACTCC GTGGGCTCCT GTGCGGCCCG AGCCTCCCCG ATGAGCGCCG 120 CCTCCTGCTC CACGGCGCCC AGTCCCATCG ACCATCCAAG GGCTGAGGAG TGCAGGCACA 180 CGGCGCGGGA CTGGCAGGCA GCTCCACCTG CAGCCCCCGT GGGGGATCCA CTGGGTGAAG 240 CCAGCTGGGC TCCTGGGTCT GGTGGGGACG TGGAGAACTT TTATGTCTAG CTAAGGGATT 300 GTAAATACAC CAGTCGGCAC TCTGTATCTA GCTCAAGGTT TGTAAACACA CCAATCAGCA 360 CCCTGTGTCT AGCTCAGAGT TTGTGAATGC ACCAATCCAC ACTGTATCTA GTTACTCTGG 420 TGGGGACTTG GAGAACCTTT ATGTAGACAT AAATCTAGCT CAGGGATTGT AAATACACCA 480 ATCGGCACTC TGTATCTAGC TCAAGGTTTG TAAACACACC AATCAGCACC CTGTGTCTAG 540 CTCAGGGTTT GTGAATGCAC CAATCCACAC TCTGTATCTA GCTACTCTGG TGGGGACTTG 600 GAGAACCTTT GTGTCCACAC TCTGTATCTA GCTAATCTGG TGGGGACATG GAGAACTTTT 660 GTGTCTAGCT CAGGGATTGT AAACGCACCA ATCAGCGCCC TGTCAAAACA GACTACTTGG 720 CTCTACCAAT CAGCAGGATG TGGTGGGGCC AGATAAGAGA ATAAAAGCAG GCTGCCCAAG 780 CCAGCAGTGG CAAGTGCTTG GGCCCCCTTC CATGCTGTGG AAGCTTTGTT CTTTCTCTCT 840 TTGCAATAAA TCTTGCTGCT GCTCACTCTT TGGGTCCACA CTGCCTTTAT GAGCTGTAAC 900 ACTCACCGCG AAAGTCTGCA GCTTCACCCC TGAAGCCAGG GAGACCACGA ACCCATCCGG 960 AGGAACGAAC AACTCCAGAC GCGCGGCTTT AAGTGCTGTA ACACTCACTG CGAAAGTCTG 1020 CAGCTTCACT CCTGAGCCAG CGAAACCACA AACCCACCAG AAGGAAGAAA CTCCGAACAC 1080 ATCCGAACAT CAGAAGGAAC AAACTGCGAA CACGCCGCCT TTAAGAACTG TAACACTCAC 1140 CGCGAGGGTC CACGGCTTCA TTCTTGAAGT CAGTGAGACC AAGAACCCAC CAATTCCGGA 1200 CACACGACCA CACCTGGCTA ATTTTTGTAT TTTTTGTGGA GACTGGGTAT TGCCATCTTG 1260 CCCAGGCTAG TTTCCAACTC CTGAGCTCAA GCAATTTGCC CACCTCATCC TCTGGAAGTA 1320 CTGGGATTAC AGGCATAAGC CACCATGTCT GGCCTATGCC CCCCTCTCTC TATATATACA 1380 TAAAAAAAAA 1390
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