Tag | Content |
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EnhancerAtlas ID | HS187-13730 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:102918210-102918890 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr2:102918373-102918383 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr2:102918373-102918383 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr2:102918373-102918383 | ATTTTCCATT | + | 6.02 | Stat6 | MA0520.1 | chr2:102918479-102918494 | CACTTCCTCAGAAGC | + | 6.23 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 102918302 | 102918766 | chr2 | 102918428 | 102918763 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I102301 | chr2 | 102918428 | 102918763 |
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Enhancer Sequence | TCTATAAATA TTTGAGCTGT GCTCTGAATT ACTGTTATGT TGCCCTGAAA CAAGTTTGAC 60 ATTTTTGGGT CTTCCTTTTA AGTTTTTTTT ATGTGTAACC AGAGTGACAT TTAGCCTGTG 120 GTTAATTTAT ACTACTATTG AGACAAAACT CATGAGTTAT GTCATTTTCC ATTTTGAATA 180 GTGGGCACAG GTACTATTTC TGACCCTGTA AGAGTTGTGG TAATTGTTCC CTCTGATCGT 240 TTTGGGTGGT TCTTTCTTTG ACCACAGATC ACTTCCTCAG AAGCATGAAC TCGTCAGTAC 300 TGAGCTGAGT AACTGAAGAG GGCGCTGCAG ATATCTCTGT AGTGATCTCC TCAGTACTCT 360 GTGAACTCAA GTCACCTTAG CCTTTCCAGA CTCCCAGCTC TGATTCCTCA TCTCGGAGAG 420 ACCACTGGAC TTCATCTCTC TTCCTCTTCT CTTTGCCAGA GTTCAGAAAC TCTCCAGGCA 480 GTAACCAGGG CAATTGCCAG CCTCTTTTTT TGCTTCCCAT CTCTCAAGGT TCACCGTCGT 540 CCACTGCCTG ATGCTTATAT CTTGAAAGCT GTTGATTCAT ACGTTTTGTT CAGTGTTTAG 600 TTATTTAAGT CAGGAGGGTA AATCTTATTC CTATTACTCT ATCTTGGCTG GAAGTAGAAA 660 TCACAAAACT TGCCTCTAAA 680
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