Tag | Content |
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EnhancerAtlas ID | HS192-14398 |
Organism | Homo sapiens |
Tissue/cell | U2OS |
Coordinate | chr9:139251000-139252460 |
Target genes | Number: 36 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr9:139251826-139251846 | CTCCAAACCAGCCCCACCCA | + | 6.52 |
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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 | AGGTGGGCTG CGGCCCTGGG CGGGCGTGGC TCGCGGCCCC TTTGCCATCC ACGTGTGTGG 60 AGGCAACTTG TGTCCTGAGG GGTGAGGTGG GCGCTGGTTC TGCCATCTCC GGTCATGTTT 120 GAGGGACTCC TGGGGGACTC AGCCAGTGTC ACCACATGAC CAGGGGTGTC TGAGCCTGAA 180 GCCCTACTCC TGGGAACCCC GGGCTGCTGG AGACACCAGA GACCCCCCCT GGCAACCCCA 240 GGACACTCCC AGGCTGTGCC ACCCCCCTGC CATGCAGGAA CTCGGGGTGG GGGCTGGGGG 300 GTCACAGGTC CTGGAGCTCA TGGCCTCAGG GATTCCCCAC CAGCCCTCCA CACCCGGCAG 360 GGAAAACACG GGCCAGATAG CACCCCCAGA GTGGGGAGGG CAGGGGGATC CAGGGCTGCC 420 AGCTGGCTGG TGGGACAAAA ACAGGGACCA TCCAGGGACC ACACAGTGGA CGGCATGGGC 480 GGAGGGTCCA GCCCCAGAGG GCAGAGCCAG GGCCGGGGCT CCAGCCTGGC AGCCACGCCA 540 GGAATGACCT CCTCATCTGT GTGGGGGTGA GCCAGGTAGG GTGGCCGGAG TGGAGACTGC 600 TGAGCCAACT GCTATCCCAA CTAGGACCTC AAACTCTGGG GGTCTCGCCA TCCCTGTGGG 660 GTGCAGCCAT TGCTGGGAAG GGGTTCAGGG TCCGTAGACT TGGGAACAGG CTGGGGGTGG 720 AGGCCGCTTG GCCCACCACG AACCAAGCCA GCACGTTTCC AGGTCTGCCG TCCTCCCCAC 780 AGCAGAGAGG AAACCTCGGC CCGGGGCCAG GCGTCCGACC AGCCACCTCC AAACCAGCCC 840 CACCCAAGAG GCCCAGAGTC CCCCATCCAC ACGCATGCCT GCGCCAGCTC CCGTCCCTCC 900 TGCTCCAGGC GCTTCAGAGA AGCCCAGACA ACCCCTTGGC CCCCTGGCCT GCACACTGGA 960 GCAGGCGAGG CCCACGGGGT CAGCCACCTG ACACAAGGGG AAGCCCTGGG GGGCGCCACA 1020 CTTCGGGCTC TGGAAGCTGA GACCTCAGGC CTGCCAGGGT CAGTCCCAGG CTGTGCTGGT 1080 TTCCAGGGCT GGGCAGAGGG ACGGCCACGC ATGCCCGTCC CTGGGGATCA GCAGATGTGG 1140 GGAGCAGGCA TCCAACGCCG CCCTAGCCAC TGTCTCCTGG GCCTGGCACA CCCATGCCCA 1200 GTGGGAATCG CTGGACCTGC TTTTCCTGGG CGGGCCTGCC CTGGGCTCCT GCGGGTTGGT 1260 GGCGGGGCCA CCAGAAGACT GCGCTCAGGG CCCGGGCTCC CAGCACAAGA CCCCAGAGCG 1320 AGGCAGGCCC CAGAACCAAT TTCCTGGGTG GACAGGGGGA AGCCCGTGAA CAGTGCACGC 1380 TGGCCTCTGG AACCACCGCT GCTGACCAGC CCCGGACCAC TGGGGCTGGG GGGGTGAGGC 1440 CGCCAACTGC ACTGTGTCCA 1460
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