Tag | Content |
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EnhancerAtlas ID | HS087-04856 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr12:10305770-10306950 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr12:10306717-10306729 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr12:10306721-10306733 | AAACAAACAAAC | - | 6.32 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH12I010152 | chr12 | 10305421 | 10307199 |
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Enhancer Sequence | GGACACTCTT ACTTTTTAAT TGGCAAAATT CTTTCTCTTC TGAGAGGGCT GGTATTCCTT 60 TAACTGTGGT GTAAGTTGAA TATAGTCATT TGCTTCATTT ATGAGTGCTG TCAGAGGGCC 120 AAGGCTCTGT ACAAGATCTT TGTGGCTGGA TTCTTGCCCT GAGTTTCACA GACCAATATT 180 TAATATATTG GCAGAATATT TTTGGTGTAA TTTGGGCTAT CATCCAGCAG ATGGCGCATA 240 AGAGTAACGG CCAGCGCTGC GGGTTTTTAC GTTTCAGCGA GCTCGCAACA ACGTCCTGTG 300 GTGTGGCCCA GCGCGGGGAG CTGACCCCAC CAGCTCCGCT CTCAAGCCTT CGGAGAGTCC 360 TCTCCAGTCA CTATCGTCAT TCCCGCATTT CCTTTGCTAG GCTGTCCGGG CTGGGCAGCT 420 CCCTCAGGCG GACACCCATG GCTGGCAGAC CTTCCGCGCC TGCCCCTAAT CTGGGCATAT 480 CACTCCCTCG GTTTTCTGAG ACTCGGGACT CCTTGCCCGC TGGAGCGCAG GCCATGAATC 540 TGGGTCCCGC ACTGCGGCGC TGCACGCCGC AGCCCAGGGC TTTGGCCCCA GCCAGCACAT 600 CCGCCATCCT GCACCCCAGG TTCCGGCACG GGCTGCGACG GGGCCTCGGA ACTGCTCCCA 660 AGCGGCTGGG AAAGAACTCA GTCAGGCATG TCGGCCTGCA AAGCACCCAG GATGGGCAGT 720 GGAGTCTGCA CCGTTGACAG GCTCCTAGAG CGGCCAGGCA GAGGACTTGA GAGGGGCTGG 780 AGGGCAGGAG GTCCTGCGGA ACAGAAGTGC CCCACTCCGA AGGGAAAGTC GACCCTGCTG 840 TTCTCTTTGC GCGGCAGTCA GTGGGGTTAG AGTTATTCGG AAGAGGACGG AGAGCCTTGG 900 GGGATGGGTG CGCATGGCCA TGTTCCACTG GAACTGCCCC CAACGCAAAA CAAACAAACA 960 AACAACAACA ACAACAAAAA CCGGGCTCTA TGCAGGCTGG AGTTCTGCCT CTGCCTGCTT 1020 GTAGGGCATA TCCCCATGCC AGTTCGAATG TTTATGGGGA GTGTAGGATC TCTTGTGGCT 1080 GGAATCCTAG AGGTCCACAG CAAGAGTGGG CTGCCTTGCC AAGGGTTGTT CAGGGCCAGG 1140 AACTGGCACT GGTGTTCCAG AACCTGAAAG GGTTCCCGGT 1180
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