Tag | Content |
---|
EnhancerAtlas ID | HS167-06474 |
Organism | Homo sapiens |
Tissue/cell | Retina |
Coordinate | chr7:44254960-44256740 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX1 | MA0509.2 | chr7:44255702-44255718 | GGTTGCCATGGAGACA | + | 6.09 | RFX1 | MA0509.2 | chr7:44255702-44255718 | GGTTGCCATGGAGACA | - | 6.1 | RFX2 | MA0600.2 | chr7:44255702-44255718 | GGTTGCCATGGAGACA | - | 6.24 | RFX2 | MA0600.2 | chr7:44255702-44255718 | GGTTGCCATGGAGACA | + | 6.46 | RFX5 | MA0510.2 | chr7:44255702-44255718 | GGTTGCCATGGAGACA | + | 6.03 | ZNF263 | MA0528.1 | chr7:44255457-44255478 | GGTGGAGGAGGAGACTGAGGG | + | 6.53 | Znf423 | MA0116.1 | chr7:44256145-44256160 | GGCCCCCATGGTGGC | + | 6.14 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAAGATCGCG CCACTGCACT CCAGCCTGGG CGACAGAGTG AGGCTCCCTC TCAAAAATAT 60 ATAAAAATAA AAGCGATGAA TGAAATGCCC GTCGGTGGTG TCCTTTTTGC CTGTAGCGCT 120 TGGCCCAGTA CAGGGTGGCT TAGCCCTGTG TGCTGTGCCC TAATACCTCA TCAGAGTTGC 180 TGCCCTGATG GCATCTGCAG AAGGGCCTCA GGAATAATGC ATGTGAGGGC GCACGATCCG 240 CAGTGCCTGC AGCCTTCCTG GGGGAGGCCT GGCCTGGAAA GCCTCCTCCG ATTACAGCTG 300 ATAGGCAAGT GGAGCCCTAG ATACCATGCT GGGGACAGAC ACTGCAGCAC TCGTGGGCAC 360 TGGCCTAGAT TCTTTGCACC TGGCTCTTGG GACCTGCCAC CTGCCCACCC ACACACCTGA 420 GAGCACCTGT CCAGGTGCAG ACCATGGGGA GCAAGAAGCT GACATCCAGG GCCACTCTGC 480 CGCGTGAAGG TGCTCAGGGT GGAGGAGGAG ACTGAGGGCT TTAGCCAGTT CTGGGGGATC 540 CTTCAGGCTC CTTGCCCATA GTGGATAGGA CTGAGAGTGT GTAGGGGCAC TCGTCTTGTC 600 AGAAGTTACT TGGACCCAAA ATGCAGGTGT GTTTAGTGTC TGGGACTGTT TTGAAGCCCA 660 TCCTTCTGTT TAGGAAAGTG CCGTGGCACT GCCTGGGACA CAGGTGTGGA GGGGAGCCAA 720 GGGCAGGGCC ACACTCTGAG CAGGTTGCCA TGGAGACATG AGGGTGCATC AGGGGGCCCA 780 GCGGGGGCCA CGAGGGTGCG TCGGGGAGGG AGGAGGGCAT TGAGGCTGAG AAGGGCCAGC 840 ATAGCACAGG CAGGTGCAGT TGCTTTCCCA GGCTGGGCCT GAGCGTGTGC CCCATGGGGC 900 CAGGCAGCAT AGGTGGTGGG TGGAGCCTGA GGACAGGAGA AACTTGGCAG GGGGTTACTC 960 CTTACTCCAA CCTAAGAGTT TGCGCTTAGC TTGGGCTGGA GATGCAGAGG GAAGGCCTCA 1020 GGGGTGCCTG TCTCCTTCAC ACCCAGGACG AAGTCCCCAA GCCTGGCCTG GCCCACAGGC 1080 CTGTAGCACC TGGCCAGTCT GGCCTGGTAT CTGGCTTCCC TGTCTCCATT CCAGCTCTCT 1140 GTCCTGGATT CTGGGCTGGT TGTGTGGCCT CTGCTGGAGC CTCCTGGCCC CCATGGTGGC 1200 TGCCTACTGT ATCACCTTGC GCCTTGCCTA TGTCTGGTGC CCGAGGCTGA TGTCCACACA 1260 GGCCTGCGTG CCATCTGTCT GCATAATCCA CTGGGGTGGA GCCCGGCTCT GTGGTCACTG 1320 TGTGTCCTCA GCATCCAGAA TAGCCAATAC ATGTAGCAGG GGCGGAAGGA AACAGCAGGA 1380 CAGCCAGAGG TCTTGGTCCT GGGGCTCCTT CCTGCCCAGA GGCTGCCCTG GCCACATCCT 1440 TAGCGGCCAC CGGGGGTGAA TGGAGAGGTC AGGGGTGTTG GGGGCTGGGA TCCAGTTTCA 1500 GTTCCAGCAT TCAGGGTGGA CAGCGCTGGG CCCAGAAGAC TTCAGAGGAC CAGAGGAAGA 1560 GGTGGAGACA GCTGGTAGAG CTATGATCTA TGACTAGTGC CCTACCTGGG GTGAGCCGTT 1620 CACCCTAGAG GGGCTCAGGA CTGTCAGGGC CAGCTCAGGG CTCCCATAGC ACTACCTTTC 1680 ATTGGAGGAG GGGCCCAAGT AGGGTCTTGG CCAGGGACCG GGCTTGAGTC TGTATTTTGG 1740 CGCAGGAGGT CGGCAGGATT CCAGCTAAAG CACCCAGCTG 1780
|