Tag | Content |
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EnhancerAtlas ID | HS051-14990 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr2:26138970-26139900 |
Target genes | |
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 | GAGAACCTTT ATGTAGACAT AAATCTAGCT CAGGGATTGT AAATACACCA ATCGGCACTC 60 TGTATCTAGC TCAAGGTTTG TAAACACACC AATCAGCACC CTGTGTCTAG CTCAGGGTTT 120 GTGAATGCAC CAATCCACAC TCTGTATCTA GCTACTCTGG TGGGGACTTG GAGAACCTTT 180 GTGTCCACAC TCTGTATCTA GCTAATCTGG TGGGGACATG GAGAACTTTT GTGTCTAGCT 240 CAGGGATTGT AAACGCACCA ATCAGCGCCC TGTCAAAACA GACTACTTGG CTCTACCAAT 300 CAGCAGGATG TGGTGGGGCC AGATAAGAGA ATAAAAGCAG GCTGCCCAAG CCAGCAGTGG 360 CAAGTGCTTG GGCCCCCTTC CATGCTGTGG AAGCTTTGTT CTTTCTCTCT TTGCAATAAA 420 TCTTGCTGCT GCTCACTCTT TGGGTCCACA CTGCCTTTAT GAGCTGTAAC ACTCACCGCG 480 AAAGTCTGCA GCTTCACCCC TGAAGCCAGG GAGACCACGA ACCCATCCGG AGGAACGAAC 540 AACTCCAGAC GCGCGGCTTT AAGTGCTGTA ACACTCACTG CGAAAGTCTG CAGCTTCACT 600 CCTGAGCCAG CGAAACCACA AACCCACCAG AAGGAAGAAA CTCCGAACAC ATCCGAACAT 660 CAGAAGGAAC AAACTGCGAA CACGCCGCCT TTAAGAACTG TAACACTCAC CGCGAGGGTC 720 CACGGCTTCA TTCTTGAAGT CAGTGAGACC AAGAACCCAC CAATTCCGGA CACACGACCA 780 CACCTGGCTA ATTTTTGTAT TTTTTGTGGA GACTGGGTAT TGCCATCTTG CCCAGGCTAG 840 TTTCCAACTC CTGAGCTCAA GCAATTTGCC CACCTCATCC TCTGGAAGTA CTGGGATTAC 900 AGGCATAAGC CACCATGTCT GGCCTATGCC 930
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