Tag | Content |
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EnhancerAtlas ID | HS136-08246 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr17:41685750-41686150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr17:41685817-41685830 | ATATGCAAATTAA | - | 7.34 | Pou2f3 | MA0627.1 | chr17:41685815-41685831 | TCATATGCAAATTAAG | + | 6.57 | RFX1 | MA0509.2 | chr17:41685923-41685939 | TGTTGCCATGGCAATG | + | 6.14 | RFX1 | MA0509.2 | chr17:41685923-41685939 | TGTTGCCATGGCAATG | - | 6.17 | RFX2 | MA0600.2 | chr17:41685923-41685939 | TGTTGCCATGGCAATG | - | 6.66 | RFX2 | MA0600.2 | chr17:41685923-41685939 | TGTTGCCATGGCAATG | + | 6.67 | RFX5 | MA0510.2 | chr17:41685923-41685939 | TGTTGCCATGGCAATG | + | 6.92 | RFX5 | MA0510.2 | chr17:41685923-41685939 | TGTTGCCATGGCAATG | - | 7 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I043608 | chr17 | 41685770 | 41686110 |
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Enhancer Sequence | ATAGGCAGTG TGCCCAGAGT GGCAGCTCAG AGGCAGTTCT GCAGTCATAT TTATACCCAC 60 CTTAGTCATA TGCAAATTAA GGGGCAGAGT ATGTATGCAG AAATTTCTGA AAAATGGGTG 120 GTAACTTCTA AGTTGTCAGG TTGTTACCAT GGAAAGGGAC AGTAACTTCT GGGTGTTGCC 180 ATGGCAATGG CAAAGTAACA TGGCACAGTG GAGGCCATGT CTTAAAGAGA GGTGCTTTCC 240 CCTCCTTCCC TGTTTTAGCT ATTACTCAGT CTGATTCATT GCTGAGCCCC ATCTCTGGAG 300 TCAAGTCCCA CCTCCTACCT CAACATGACC AAATCTAACT GCAAGCAAGG CTGGGAAATA 360 TAGTCTCTCT TGGGCAGCCA TATGCTCAGC TGAAATTCTA 400
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