Tag | Content |
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EnhancerAtlas ID | HS060-17165 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:12404480-12405500 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr19:12404654-12404674 | CCACACACAAACCCCACACA | + | 6.06 | RREB1 | MA0073.1 | chr19:12405060-12405080 | CCACATCCCAACCACCCCCG | + | 6.21 |
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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 | AAGTTAGCAT ATGGAAGGCT CTGGAAACCA AAAGATTTAC TGTTAGCCCC AAGAGGAGTT 60 AGGATGAAGG GACAGGTCTC AAAGACCCTG ATGCCAATAT CTTTGAAAGC CTCGGAGGAG 120 AAATGGTCGC CCTTGGAAAG AAAGGACTGA AGAGCACAGA GACCACAGCT CCTCCCACAC 180 ACAAACCCCA CACACGAGTC TGGTTTGTGC CTAGTGACCC TCCCACCGTC ACCGTGCAGC 240 CTCCTCACCG GGCTCACAGG AACTGCGAGC CAGGCTGGAG GCGAGATTGC AGTTAGATAT 300 TAACCAGGTG CCCTCAGCCC CGCTGCTTCA CAGGAAGCCG CCTCCCTGAG AGTCAGGTCA 360 CAGCAGACGC TGACCGCCGG CTTCCCCATT GGCCTGGGGA TAAGATCTCT GAGAGTTGCT 420 CAAGAGTCGT CTAAGTTCTT TCTCAGATCT TGAATTCCAG CGGAAAGGCT GGCGCCAAGC 480 AGGCTGAAGA CCCCACAAGG AAGCCCACTC AGCAGCAGAA TGCGGTTTCT TCACCTCCAG 540 TCCCAAGATT CACCCCTCAC TTCTCCACCA ACCAGCGACC CCACATCCCA ACCACCCCCG 600 TCCAGACCCC TAAACACCCC ATCCTCAAAC CTCTCACGGA GGCGGATCTA GGGTGTCCTC 660 TCCTATTAAA CCGTTTCTGC TGCAGCCCTC GGCGTCCGGG TGCAGTGACT TGGGCTGCGA 720 ACCTGTACTG GTTCCGCCGC ACAATCTGGG GAGAAGCGGG GCTGAGGGCG CGGAGCTGCC 780 CAGAGAGGGG CGCCGGGGCC GGGGCCGCAG TCGCAGCTCA GGGACGGGAC AGGACGCCCG 840 GGGTCCCGGC TGCCGGCCCA GCCCCACCCT GCGGCCAAAC GGACCGAGGA CCGAGGTGCG 900 CAGGGGGCGC TCAGGTCCCA GACCCCAAAG ACGCTGCGGC GAGGCCCGGG TCCCGCCACA 960 GCCGGTTCCG ACTGGTTCCG ACCAGCCCTT CGCCCTGCCT CAGGACGCCG GGCCCCGCAC 1020
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