Tag | Content |
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EnhancerAtlas ID | HS051-13745 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr19:12404380-12405500 |
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 | CATACATTGC TATCTGAAAA CAAACGACAA AATTCTGTGT CTATTTGAAA TATCGTCTTG 60 CTGACAAAGG GTTCATAACG TTACTGGGAA TTGAGGAGTG AAGTTAGCAT ATGGAAGGCT 120 CTGGAAACCA AAAGATTTAC TGTTAGCCCC AAGAGGAGTT AGGATGAAGG GACAGGTCTC 180 AAAGACCCTG ATGCCAATAT CTTTGAAAGC CTCGGAGGAG AAATGGTCGC CCTTGGAAAG 240 AAAGGACTGA AGAGCACAGA GACCACAGCT CCTCCCACAC ACAAACCCCA CACACGAGTC 300 TGGTTTGTGC CTAGTGACCC TCCCACCGTC ACCGTGCAGC CTCCTCACCG GGCTCACAGG 360 AACTGCGAGC CAGGCTGGAG GCGAGATTGC AGTTAGATAT TAACCAGGTG CCCTCAGCCC 420 CGCTGCTTCA CAGGAAGCCG CCTCCCTGAG AGTCAGGTCA CAGCAGACGC TGACCGCCGG 480 CTTCCCCATT GGCCTGGGGA TAAGATCTCT GAGAGTTGCT CAAGAGTCGT CTAAGTTCTT 540 TCTCAGATCT TGAATTCCAG CGGAAAGGCT GGCGCCAAGC AGGCTGAAGA CCCCACAAGG 600 AAGCCCACTC AGCAGCAGAA TGCGGTTTCT TCACCTCCAG TCCCAAGATT CACCCCTCAC 660 TTCTCCACCA ACCAGCGACC CCACATCCCA ACCACCCCCG TCCAGACCCC TAAACACCCC 720 ATCCTCAAAC CTCTCACGGA GGCGGATCTA GGGTGTCCTC TCCTATTAAA CCGTTTCTGC 780 TGCAGCCCTC GGCGTCCGGG TGCAGTGACT TGGGCTGCGA ACCTGTACTG GTTCCGCCGC 840 ACAATCTGGG GAGAAGCGGG GCTGAGGGCG CGGAGCTGCC CAGAGAGGGG CGCCGGGGCC 900 GGGGCCGCAG TCGCAGCTCA GGGACGGGAC AGGACGCCCG GGGTCCCGGC TGCCGGCCCA 960 GCCCCACCCT GCGGCCAAAC GGACCGAGGA CCGAGGTGCG CAGGGGGCGC TCAGGTCCCA 1020 GACCCCAAAG ACGCTGCGGC GAGGCCCGGG TCCCGCCACA GCCGGTTCCG ACTGGTTCCG 1080 ACCAGCCCTT CGCCCTGCCT CAGGACGCCG GGCCCCGCAC 1120
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