| Tag | Content |
|---|
EnhancerAtlas ID | HS167-02888 | Organism | Homo sapiens | Tissue/cell | Retina | Coordinate | chr2:71169560-71170780 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr2:71170455-71170475 | AGGGAGTGGGTGAGGTGGGG | - | 6.26 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTCCTGGTGA AAAGAGCTTA GATCAAACAA AAAGAAGAAG CTTGACCACA CATATCCAGA 60
CTGGGAAGGG GAGGGACTTT TGGTTTTTCT TTGGCATGGG GTGGCTCGGG GCCAGGCTTG 120
CCCAAAGCAA GAGGGTAAGT GAACCGAGAA CCAGTGTGGT CCAGCAAGAA GCACAGGGTG 180
GGTTCCCAGC CCCAGCTCTG CTACAGATGT GCTGTGTGGC CCTGGGCAAG GCTTCTCACA 240
CTTCTGGGCC CCATTTTCCT TGCCTGTGAA AGAGGGGTTG GGCCACTCCC CTCTGCATCC 300
TGCCAGCCTG TGGCTGACCC AGAGGCCTCA CAGACCCCCT GCCCACCTTG CCAAATGCCT 360
TCATCTCAGG TGTCTCATCT CATTGGTGCA TCACAAGAAC CTCAGAGAAG GGCACTGGTC 420
AGGACTATGG GCAAGGGACT GTCCCAGGTC TCTCAGCCAG CCTCTAGCAG AACCAAAACT 480
AGGCTTGCCT CCCGCAAGTC CACAGCTTCT TCTATGGGAG TTAGGAAGTA TTTTTTGGCA 540
TCTAACCCAA TTCCCTATGC AAGCTGAGCT CATTTGCCAT GTGTGGGTCT CTGCAGCTGC 600
CACATCTGCA GGCATTTCCC TCCTTCCCTT GCCTTTTCAC TCCCTCCCCT CCCATGCTGA 660
GCACCCAGTG AGCCTGGGGA GTCCAGGAAC CTTGTGATGA GAGCAGAGGC CCCGTCTGGT 720
TTTTCTCACT GACGTCTGCA CCCCCTACAC ACCACATACA CACACACACA CACACACTGC 780
TCAATCAGTG TGGGGTGAAT GGAGGGAAAT GCAGTCCTGG TGAGGGCAGA GGAGGGCACT 840
TTTCGGCCAC AGCCGGGGGC CAGGAGCTTT TGGAAAATGC TTGGAGTGAG AGAGGAGGGA 900
GTGGGTGAGG TGGGGGTTGA AGCCAGAGGG GAAGCAGCCT CAGGGATGAG AGGCCTCTGT 960
GTGGTGGGGG CGGACTCTGA GGAGGCCTCT GCCCTCTGCC TGGCCCTCCC CCAGCCTCCT 1020
GCAGGTGTCC GAGCAGCAGG GGCCCTGCGG GCAGGGGCAT GACCCTTACA GCAATGGTGG 1080
CTGGCCCTGT CACAGCTAAT GACCCTGACG GCCCAGGCTG GGAAGGAGGT GGGGTGTGGA 1140
GAGAGGAAGG GAAGGCAGAG GATGCCTCTG TGTGTGTGAG CAGGGTGTTT GGGGTGAGAC 1200
CCCTACTCAC CCCCGCCCCT 1220
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