Tag | Content |
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EnhancerAtlas ID | HS101-30628 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr3:127572210-127573430 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYB | MA0100.3 | chr3:127572661-127572671 | ACCAACTGTC | + | 6.02 |
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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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Enhancer Sequence | GATTACATAT ACAAAGTTCA ATAAAAAAAT TTTCACTATC TACAGCAGTT CTTTTCTGGA 60 CATTATTATT ATTCCTTTTG TTTAATGATC ATTATTGAAA AGAATTCTGT TGTATGGAGG 120 AAGGAAGCAT TAAAAACCAA TTCTTGACCA GGGGCAGTGG CTCATGCCAG TAATCCCCGC 180 ACTTTGGAAG GCCGAGGCAG GCGGTCCTGA AGTCGGTAGT TTCAGACCAG CCTGATCAAC 240 ATAGAGAAAC CCCATCTTTA CTAAAAGTAG AAAATCAGCC AGGTGTGGTG GTGGGTTCCT 300 GTAATCCCAC CTACTCGGGT GGCTGAGGCA GGAGAATCAC TTGAACCCGG GAGGTAGAGG 360 TTGTGGTGAG CCGAGATCGA GCCACTGCAC TCCGGCTTGG GCAACAAGAG CGAAACTCAG 420 TGTCAAAAAG AGAAACAAAA AACAAAAACA AACCAACTGT CTGTAAGTGA ATCACATGGT 480 AGGTCCGCCA GGTGGAGACA GCAGATTGAG CAGTCTAGTC TGCTCCTTCC ATGGCCCCTC 540 GCTGGTGATG ATAGAAGACT TGCTTTAAAG GAGAGGAAGC ACGGCAGCAC AGTCCTGGAA 600 GCTGGAACGC AGAGGGAGCA TGGAAATGAC ACACCTGGCA GCCCCAGGAA GACCAAGCCC 660 TGAGCTGGCA ATGGAGAAAG ATGAAGCTCA GCCAGACTTA CCCCACAGAA TCCCCGGAAA 720 GCCCAGGACT TCAAGGCACT CGATGTCTCT GGCAGTAGAG GTGACAAGGA TGGTGACCTG 780 GAGGCTGCAG GAAGGTTTGT TTAAGGAGAG GTCCAACACT CAGGCCCGCT CCCCACTCTG 840 CATTTTTGGT GATTGTTCTT CTCCCAACCT AGCAGAAGAC GAGAGATTTA TTTTGGGGAG 900 AGGATAAAAA GTGAGTCTTT TGCACCGGGA GCAGCAGCAG CACAGCTGAG GTCAGCGTTG 960 TCATCCCAAC ACATCTAAGT AAAAGATTAT ATGTATTTTG GATGCTGAAG TCTCTAGCCA 1020 TCTTTCCTAA TCAGTTTTTG GACGTTTTCA CCCTGAGGCC ACAAACTGGA GGATCTTTCT 1080 GGATGGAATT TGAGGGATAG CACAGGGACT ACCCCAGTGA GATGACCCAG CACAGCACGC 1140 TCCTGCCAAG CTCCAGGTTG GCAGGCCAGT CACGCCTGCA GTTTCCAATA CGTGTGTTAG 1200 TATCCCACTC CTGGGTGTGT 1220
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