| Tag | Content |
|---|
EnhancerAtlas ID | HS184-20958 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr3:133048530-133049280 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFG | MA0659.1 | chr3:133048654-133048675 | TAATTGCTGAGTAAACATGTT | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGTTTCAACA ATTCTTATCA TAGCCTGCAG GCACACAAGA GCAGGAGAAA AAGCAAATTG 60
CAAAGTGAAG ACCCAGCACC CTGTGTTTAG CCTTCACCCA AAATTGCACT GCACGGTGAA 120
CACTTAATTG CTGAGTAAAC ATGTTTCTAG GCTGTGATCT AGATTCCCTA AGAGAAGGGT 180
TATAGGATAG TGTGTGGTTA TATTCCCTCT ACCTAGAGAG GATTAAGTCT AAAATCTCCT 240
GCATCAAGAA TCTTGGTGCT GGGAAAGATG CAATACAGGT TCTCCAAGGA ATGAGTTTCC 300
ACCTGTCTTT TTATGCTTTG CATCTGGCAG TTTCCTGCTT TTGGAGAAAA AAAAATCTGT 360
GACAGCATAC AGGAGGAAAA GGAACATTAA AAATGCCATA AATACTTCTA GCTATTTACC 420
TACCCTGAAA TGTGCTAGAT CAGTTCCCTT GATGAAGACA ACTTTTTAAA AAATAAGTTT 480
CCTTTCAATA GATAAGAAGC CTTCTCTCTG CTGGCCATGC TTCCCCTGCG GAAGCCTGTG 540
GTGCAGTAGC TGCTGCTGAG ACTCCTCTGC CAGTTGCTAT GGAGAGCAGC TGCAGGGGAG 600
GGGATTCCTG GAGAGGCAAA GAGGTGGAGA GGAAGCTCTC CTGTCTAAAT CCAGATTCTC 660
CATCTGAAAA GGTTAAGCAG GAGGGAAACA ATATTCAAAG ATGGGTGTGG GTTTGGAGGT 720
GGGGTGTGTA TATATGTGTG TGTAAGAGAG 750
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