Tag | Content |
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EnhancerAtlas ID | HS101-45299 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr9:72260040-72260990 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
USF1 | MA0093.2 | chr9:72260682-72260693 | GGTCACGTGGC | - | 6.62 | USF2 | MA0526.2 | chr9:72260679-72260695 | ACAGGTCACGTGGCAT | + | 6.09 |
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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 |
GH09I069645 | chr9 | 72260621 | 72260770 |
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Enhancer Sequence | TTTAAGATCG ATGTTGGAAG GGAAAGGAGA TACTGAGAAA TTAGTCGAGG GGTTGAATAA 60 GTATAACTTG TATGTTTTTT ATTACCTCCA AAGCATTTTC ATCTTACTTG ATCCTTACTG 120 GCTCATGGGA TAGGTAAGTA AGAAAGGCTG TAACTTTGTC CAAGCCACAG AGGCCAACAG 180 AATTGAGGTC AATTTCTCTA ACATGATTGA ACAGGAAGCT GTTTAGTTAT TTGAAAACAT 240 CAGTTAAGGC AAGATCTCAT AACAACATGA CACAAGCAAA ACATTTTTCT TTCATTTGGC 300 CACTCACTGC CTGAACCGAG TTATGTGTTT GGCAAGTTCA CCACTTTGTG AGTCCAGGTT 360 GGGCGAGGCA AGATCGTCTA CCTGAAGTGA GAGAAAAAAA GCTAGAGACT TGCTTGCCCA 420 GTTTCCCTTG CAGCTAGAGA AAAGGCTGAG GGAGAAGTGA GCTCTGCCAA CCAGGCAGCC 480 TGCACGGAGG CGGACTGGGA GCTTACATTA TGAAAGGGAG GGGGGAGCTC GTGCTCTCTT 540 CAGCAGTGGC AGGAGAAGGG TGGCCTTGTA GCTGCACACT CGACACAGAG GTAGCTTTGA 600 GGATGGCAGG GCCAGCAGCT GCGATTAAGG TCCTGGCAGA CAGGTCACGT GGCATCGAGA 660 GCTCCCTAGA GGTGGCACTT TCTCGTCAGA CCAGTTCTGG GGTTTGGTGT TGGGTGCTGC 720 TCCAGGAAGC TCAGCCTTCA TTCAGACTCT CCAGTTCTCC CAATTCTCCA GCTGCCCAAT 780 CACGTCTCTG CTTAGCCAGA GTCATTTTCT GTTGCTAGTG TCTAAGAACT CTGACTGATA 840 CACCTTAAAA CCATAAATGT TTTGTTTTAC TTTAAATATC ACATGGATAG ACATACTCAC 900 CAATCTTAAC ACCAGTTGAA AGTAAGTCCT GTGACATATA AGCAAAATGA 950
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