| Tag | Content |
|---|
EnhancerAtlas ID | HS168-00131 | Organism | Homo sapiens | Tissue/cell | RPE | Coordinate | chr1:37979440-37980250 | 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 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGAACTTGGG CGATGTCCAC TCCCACGCAC AAAAGGTATC GCTACCAGGA GAGGGAAAGG 60
TGAGCAGCCT TTCAGCGTCA ACTCGCTCCC CTCCCCGCAG GCTCAAGAGA GGCCGCCGAC 120
ACCGGGCTGC CAGTTGCTAT GGAAACCTAG AAGGGCAGCT TCAGGTGAGA GGGGCCTCCC 180
GGGTGCCCAA GCCGAGACGC GGGGGCAGGA AGAGCTTAGC CACCAGAGTG CATTGGGCCT 240
TGGGTGCCTG TCACAATTCT GAATTCTCCG GAATGTGTTC TTCTCCCTCG CCTGTCACCT 300
TCTAGATGTT CCCAAACACA TCACAACCCT GTCTATCAAA AACCTCCATT CAACGGATCT 360
ACTCCCAGTA CCAAAAAGAA CACGCTCCCC ACCAGCCTCC AAAGTCCAGA CGGGGTGACT 420
GGGTCCCCCT CCCACACTAG CCTCCTTCCC CACCCCCTCC CCGCAAAGAT CACGGACTAG 480
CCCGCCTCGC CCACCCCCGC GGCTCACTGA CGCTCGCCCT TCCTAGCGCC CTCTCCCCGG 540
GCCCCGGCAC CGTCCTCCCT CCACGCCCCC TCCTGCGGCT GCCGCTTCCC CTCCCCCTCC 600
CGCGCTCCCG GCTCTCTCCC GGCTCCGGAT TCGCACAGCC GGGAAGCTGA ACCGCCGGCG 660
GGCCGCAGAA TGCGCACCCG GCCTCAGGCC GCCGAGCACC CGGCCCGCCG CGCCGCGCCC 720
CCGGAGTAAC AAACGGCCTA GCGCGGCCGG GCTTGGGGCC TGGAGGCGGG GCGGGCGCGG 780
AGCCCCATGC CGTGCAACCC CTGTCCTAGC 810
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