Tag | Content |
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EnhancerAtlas ID | HS187-12980 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:26139110-26139860 |
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 | TCTGTATCTA GCTACTCTGG TGGGGACTTG GAGAACCTTT GTGTCCACAC TCTGTATCTA 60 GCTAATCTGG TGGGGACATG GAGAACTTTT GTGTCTAGCT CAGGGATTGT AAACGCACCA 120 ATCAGCGCCC TGTCAAAACA GACTACTTGG CTCTACCAAT CAGCAGGATG TGGTGGGGCC 180 AGATAAGAGA ATAAAAGCAG GCTGCCCAAG CCAGCAGTGG CAAGTGCTTG GGCCCCCTTC 240 CATGCTGTGG AAGCTTTGTT CTTTCTCTCT TTGCAATAAA TCTTGCTGCT GCTCACTCTT 300 TGGGTCCACA CTGCCTTTAT GAGCTGTAAC ACTCACCGCG AAAGTCTGCA GCTTCACCCC 360 TGAAGCCAGG GAGACCACGA ACCCATCCGG AGGAACGAAC AACTCCAGAC GCGCGGCTTT 420 AAGTGCTGTA ACACTCACTG CGAAAGTCTG CAGCTTCACT CCTGAGCCAG CGAAACCACA 480 AACCCACCAG AAGGAAGAAA CTCCGAACAC ATCCGAACAT CAGAAGGAAC AAACTGCGAA 540 CACGCCGCCT TTAAGAACTG TAACACTCAC CGCGAGGGTC CACGGCTTCA TTCTTGAAGT 600 CAGTGAGACC AAGAACCCAC CAATTCCGGA CACACGACCA CACCTGGCTA ATTTTTGTAT 660 TTTTTGTGGA GACTGGGTAT TGCCATCTTG CCCAGGCTAG TTTCCAACTC CTGAGCTCAA 720 GCAATTTGCC CACCTCATCC TCTGGAAGTA 750
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