| Tag | Content |
|---|
EnhancerAtlas ID | HS184-18332 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr20:46537220-46538760 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr20:46538145-46538159 | TGATGACGTGGAAT | - | 6.81 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH20I047909 | chr20 | 46538641 | 46538730 |
| Enhancer Sequence | GGAGGCTCCC CAATACCCAT CTCCCCGATA ATGGCCAATG CGCCTCAAAG GGTCACTTCC 60
AAAGAATGCC AGGTGGCAGG CACCAGGTTT TGGCATCTGA TACGCTCCCA TCCACTCCCT 120
GGGGACCTAA GCAATCATCC TTTATAATCT CTGACGGGGA ACAACTGGCC GTTGTCCTTT 180
AATTAGCAGG GGACACACTA AGCTATGGTC TCCTGCAGGC TCCATAAACA TCCGTGAAAT 240
CAGCCTGGTG ACTCCAAGCT CGGTGCAGAC TGCGGGGGCC CACAGAGGCC AAGGGGAGCC 300
CCCGCCCCCG GTCTGGCTCT GAGAACAGCC TCCAGGAGAA ACTGCCAAGC CACCCGGACT 360
CATGGCAGCT GCTTAAACTG GCAAGTTCTT TCTTGCAAAT TGAGATCCAG GCTGCGATCT 420
GGGCTGGCTC TGCACATTCC AGCCACCTGT TTTACCTGCT GGTTGGAGCT GCCTTGGTAC 480
CTCTGAGGGC TGCTTGTGTG TGGGTGGGGG CTGCTTTTGA ACACATGGCT GCCCCGTGGG 540
CCGCGCCTTC TCCACTTCTT CTGGCCTTAT AAAATGATGG TTATTGCAGG GAGGATGCAG 600
GGCCAAGCAT CCTCTTATGT AGCGCCGTGA GATGTGGGGT GTCCAGTGTC CCAGGAGAAA 660
TTCAAGCCTC ATTTCCCTCT GAGACACTGG GATGGGGCCA CGTGCAGCGT CTTAGTGCCT 720
GGATCCCAAG TGTGTCGTCT GAGTCTGTGC ATGAGGGGCC AGGGCCAGGC CTTAGGCTGT 780
GTAGGACGGA ATTGAAGCAT GTTTGATGGG AGGGCCCAGG TCACACCCAC CAGGGGCCAG 840
GAGTGCACAG ATGTAGATGC CAATGCCAGC CCAAGTCACC CAAAATGGCG AAAGTGAGCT 900
GCTGGGAAAC CTTCGGGCCA GAGGCTGATG ACGTGGAATC CTGGAGGGGA CTGCCTGCTG 960
CTCAGGGTAG AAGGGGACAT TCTGATGCGG CACCCGTGAC AGCCCTCCAG TGTTCCCGCC 1020
ACCCAGACCC ACTGTCCCTG GAGACCTGCA GAGGGAACCA CTGCTGACGA GAAAGTGTCT 1080
CCGTCACTTG CTTTGTTTCC CCTTGGTCAC TGCAAACACA TGCTCACAGC CCTCGGGTGA 1140
CAAGCCTCTT TCCGCCCCCT TCTGATGCCC CTGCTCTATG GGTGTTGTCA CTGCTCCTGG 1200
CTTGCAGTGT CCTGTGTGGC TATGACAACC TGGGTTCCTC TCAGGGCCGG TGTCCCTCCT 1260
GCAGAAAGCT CACCCTGTCT CCTGGGCCCT GGCCCTGCTC CTGGACAGAG GAGGGAAGGA 1320
CTGGGGTGGT GGCTGATGGA TTCTCATGTC ACCTCTTTCC CATATTCCCC TGGGCTCTTC 1380
CTTCAGAGCC TCCACCCTGC ACCCTGATGA CTCACTGTGT CTCATGTAGG AAGCCCCCGG 1440
TGACATCTCA TGCCCTGTAC ACAGGTCCCT ACAGCCCGGG CCCCTCCTTA GCTCTGCTGC 1500
CTCTGGGGGA AACCCCACTT TCAGCCCTCC CCCTACTCCT 1540
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