Tag | Content |
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EnhancerAtlas ID | HS074-00350 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr1:37979260-37980250 |
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) |
RFX1 | MA0509.2 | chr1:37979571-37979587 | AGTTGCTATGGAAACC | + | 6.07 | RFX1 | MA0509.2 | chr1:37979571-37979587 | AGTTGCTATGGAAACC | - | 6.09 | RFX2 | MA0600.2 | chr1:37979571-37979587 | AGTTGCTATGGAAACC | - | 6.56 | RFX2 | MA0600.2 | chr1:37979571-37979587 | AGTTGCTATGGAAACC | + | 6.57 | RFX5 | MA0510.2 | chr1:37979571-37979587 | AGTTGCTATGGAAACC | - | 6.57 | RFX5 | MA0510.2 | chr1:37979571-37979587 | AGTTGCTATGGAAACC | + | 6.63 |
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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 | TGGAGAGATG GAAGATACGG GGAGGAGGAG CCGTTTAGGA CTAAGACAGT CTAGACCTTT 60 GGGGGTGATG GACCCCTGAA TGTATAAAGC ATGTCTCCAG AAAAATACAC ACACACGCGA 120 AATTTTGCAT ATACTTTAGA GGATTCACGG AAACCATGAG TCAAGAGCCC AGGCTAACGC 180 AGAACTTGGG CGATGTCCAC TCCCACGCAC AAAAGGTATC GCTACCAGGA GAGGGAAAGG 240 TGAGCAGCCT TTCAGCGTCA ACTCGCTCCC CTCCCCGCAG GCTCAAGAGA GGCCGCCGAC 300 ACCGGGCTGC CAGTTGCTAT GGAAACCTAG AAGGGCAGCT TCAGGTGAGA GGGGCCTCCC 360 GGGTGCCCAA GCCGAGACGC GGGGGCAGGA AGAGCTTAGC CACCAGAGTG CATTGGGCCT 420 TGGGTGCCTG TCACAATTCT GAATTCTCCG GAATGTGTTC TTCTCCCTCG CCTGTCACCT 480 TCTAGATGTT CCCAAACACA TCACAACCCT GTCTATCAAA AACCTCCATT CAACGGATCT 540 ACTCCCAGTA CCAAAAAGAA CACGCTCCCC ACCAGCCTCC AAAGTCCAGA CGGGGTGACT 600 GGGTCCCCCT CCCACACTAG CCTCCTTCCC CACCCCCTCC CCGCAAAGAT CACGGACTAG 660 CCCGCCTCGC CCACCCCCGC GGCTCACTGA CGCTCGCCCT TCCTAGCGCC CTCTCCCCGG 720 GCCCCGGCAC CGTCCTCCCT CCACGCCCCC TCCTGCGGCT GCCGCTTCCC CTCCCCCTCC 780 CGCGCTCCCG GCTCTCTCCC GGCTCCGGAT TCGCACAGCC GGGAAGCTGA ACCGCCGGCG 840 GGCCGCAGAA TGCGCACCCG GCCTCAGGCC GCCGAGCACC CGGCCCGCCG CGCCGCGCCC 900 CCGGAGTAAC AAACGGCCTA GCGCGGCCGG GCTTGGGGCC TGGAGGCGGG GCGGGCGCGG 960 AGCCCCATGC CGTGCAACCC CTGTCCTAGC 990
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