Tag | Content |
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EnhancerAtlas ID | HS109-11878 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr2:26138990-26140090 |
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 | AAATCTAGCT CAGGGATTGT AAATACACCA ATCGGCACTC TGTATCTAGC TCAAGGTTTG 60 TAAACACACC AATCAGCACC CTGTGTCTAG CTCAGGGTTT GTGAATGCAC CAATCCACAC 120 TCTGTATCTA GCTACTCTGG TGGGGACTTG GAGAACCTTT GTGTCCACAC TCTGTATCTA 180 GCTAATCTGG TGGGGACATG GAGAACTTTT GTGTCTAGCT CAGGGATTGT AAACGCACCA 240 ATCAGCGCCC TGTCAAAACA GACTACTTGG CTCTACCAAT CAGCAGGATG TGGTGGGGCC 300 AGATAAGAGA ATAAAAGCAG GCTGCCCAAG CCAGCAGTGG CAAGTGCTTG GGCCCCCTTC 360 CATGCTGTGG AAGCTTTGTT CTTTCTCTCT TTGCAATAAA TCTTGCTGCT GCTCACTCTT 420 TGGGTCCACA CTGCCTTTAT GAGCTGTAAC ACTCACCGCG AAAGTCTGCA GCTTCACCCC 480 TGAAGCCAGG GAGACCACGA ACCCATCCGG AGGAACGAAC AACTCCAGAC GCGCGGCTTT 540 AAGTGCTGTA ACACTCACTG CGAAAGTCTG CAGCTTCACT CCTGAGCCAG CGAAACCACA 600 AACCCACCAG AAGGAAGAAA CTCCGAACAC ATCCGAACAT CAGAAGGAAC AAACTGCGAA 660 CACGCCGCCT TTAAGAACTG TAACACTCAC CGCGAGGGTC CACGGCTTCA TTCTTGAAGT 720 CAGTGAGACC AAGAACCCAC CAATTCCGGA CACACGACCA CACCTGGCTA ATTTTTGTAT 780 TTTTTGTGGA GACTGGGTAT TGCCATCTTG CCCAGGCTAG TTTCCAACTC CTGAGCTCAA 840 GCAATTTGCC CACCTCATCC TCTGGAAGTA CTGGGATTAC AGGCATAAGC CACCATGTCT 900 GGCCTATGCC CCCCTCTCTC TATATATACA TAAAAAAAAA TATATATATA TATATACAAA 960 CACACACATA TATACACATA TATATATATA CACATATATA TACACATATA TACACACATA 1020 TATATATACA CACACACATA TGTATATATA TATATTTTTT TTTTTAAGAG ACAGGTTCTC 1080 GGCCAGGTGC AGTGGCTCAT 1100
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