Tag | Content |
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EnhancerAtlas ID | HS129-35141 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr8:26302870-26304390 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr8:26304133-26304148 | GAGGTCAGGAGTTCA | + | 6.22 |
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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 |
GH08I026445 | chr8 | 26302918 | 26304316 |
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Enhancer Sequence | ATGCTGGTCT CCTGACTTCA AGTGATCCGC CTGCCTCAGC CTCCCAAAGT GCTGGGATTA 60 CAGGCGTGAG CCACCATGTG CAGCCAGTAG TGCTCTTTCT TTACCTCTGC CCAAATGAGG 120 ACAAGGAGAT GAAGCGTGGC TGAAAGCATC AGCCTCTTCC CAGCTGTCCT GATTGCATGG 180 GCCGCTTGTC CACTGGACAG GTACTTTTCC TGCCGGGCCT GCTCGTGTGG TTTGGACAGA 240 TGCCCAACTG TCAGGCTCAC TCTGTTCTGT TCAGGGAGCT GGCATTTGCT CCAGTTTCCT 300 CACCTGCCCA CAGGGCAGGT GTGTGTCTGT GCGCCCCAAC CCCCTTGTCT TATGAGGCCC 360 ACTCTAATCC AAAAGGACCT CATCTTTACA TAATCAGATC TGCTACGATA CTATTTCCAA 420 ATAAGGCCAT GTTCACAGAT ATATGAATGG TAAGAGCCAG TGGGCCAGGT TGCCCATGTG 480 AGGGAGCCGG TCTCCGCACC TTGAATTTCT CTACTGTTCT GGCCTCCGGG GCCATGACAT 540 TGAGGATGGC TGGCCACTGG GCATTGCTCC TTGCACCATT TTCTCTGGGA CTCCCTGATA 600 CATGTGAGGT TCTTCTTTCT CAGGCCTCTT TGAGGTGCAG GGACCCCCCC GCCCCCATTG 660 CCTAGTACTC CAAACTGGCC TAGGTCTACC TCTCCCAGCC CAAATGTCCT GAGGTCCGTG 720 ACTGGATTAT GACTTCATAA ACACCCTTCC CCCACCCTCA CCACCACCAC TTCCAGCATC 780 TGAGCTGGAA GACTGCCCGT GTCCTTCCAA TCCACTTCCC TTCCCTGTTG TTCATCCTCA 840 CATTTCTCTA ACCACAGGCC AGCAGAGCTA GAAAAAACCC TAGGACAACT AGTCCAGCAA 900 CGGCGAAACA TTCATTTTAA CCTTAGTTCA CATGGTGCAG CCGCTACAGA AAACGGTATG 960 CGAGTTCCTC AAAAAATGAA ACATATGATC CAGCAGTTTC ACTTCTGGGT TTCTGGGTAT 1020 ATTCCCAAAA AAACTGAAAG CAGAAACTTA AATAGCTGTT TGTACACCCA CGCTTATAGC 1080 AGCATTAGTC ACAATAGCCA AAAGGTAGAA GAAGCCCAAG TGTATATCAA CAGATGCATG 1140 GAGAAACAAA TGTGTATACA TACAATGGGT TATTATTCAG CTATAAAAAA GGAATGAGGC 1200 CAGGATCAGT GGCTCACACC TGTTATCCCA GCATTTTGGG AGGCCAAGGT GGGCGGATAA 1260 CCTGAGGTCA GGAGTTCAAT ACCGGCCTGG CCAACTTGGT GAAACCCCCG TCTCTACAAA 1320 AATGCAAAAA TTAGCCGGGC ATGATGGCAG GTACCTGTAA TTCCAGCTAC TTGGGAGGCT 1380 GAGGCAGAAG AATTGCTTGA ACCACGGAGG CGGAGGTTGC AGTGAGCTGA GATCGCACCA 1440 TTGCACTCCA GCCTGGTTGA CAGAGCGAGA CTCTGTCTCA AAAAAAAAAA AAAAAGGAAT 1500 GAAATTCAGA TACATGCTAC 1520
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