Tag | Content |
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EnhancerAtlas ID | HS183-14448 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr9:139297330-139298500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr9:139297411-139297431 | GGGGAGGGGTTGGTAGGGGG | - | 7.08 | STAT3 | MA0144.2 | chr9:139298162-139298173 | CTTCTGGGAAG | + | 6.14 | Stat4 | MA0518.1 | chr9:139298162-139298176 | CTTCTGGGAAGTGG | + | 6.01 | ZNF263 | MA0528.1 | chr9:139297615-139297636 | GGGGGTGGGGAAGGAAGGGGA | + | 6.43 |
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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 |
GH09I136403 | chr9 | 139297619 | 139300103 |
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Enhancer Sequence | ACCAGTTGCC TGAAAACAAG CATGGATATC AGGATGGGTG GCAGCAGCTA CTCAGCAGCA 60 ACAGGGTTCT GGGGGGAGAA AGGGGAGGGG TTGGTAGGGG GAAAAAGGGA GGGGTTCCAA 120 GGGGTAGGGA AAGGGGAGAG GTTCTGAGTG GGAGGAAGGC GAGGGTTTCC AGGGGGAAGA 180 ATGGGGAGGG TTTCCACAGG GGGTGGGGGG CAGAAAGGGG AGGGGTTGGT AGGCAGAAAA 240 AGGGGAGAGG TTCTGAGGGG GAGAAAGGGG AGGAATTCCG GGGGTGGGGG TGGGGAAGGA 300 AGGGGAGGGT TTCCAGAGCG GGGAGGGATT CCACAGGGGA AGGGTTCTGG CGGGGAGAAA 360 GGTAAGGGGT TCCAGGGAGA AAGGGACAGA ATTCTGGGGG GAGAAACAGA AGGGGTCCCA 420 GGGAGCAAGG GGTGGGGTTT GCCGGGGGGA GAAAGGGACA GGGTTCCAGG GAGCAAGGGG 480 TGGGGTTTGC CGGGGGAGAA AGGGACAGGG TCCCAGGGAG CAAGGGGTGG GGTTTGCCGG 540 GGAAGAAAGG GACAGGGTTC CTGGGAGCAA GGGGTGGGGT TTGCCGGGGG AAGAAAGGGA 600 CAGGGTTCCT GGGAGAAAGG GAGGGGCTGG GGGAGAACCA CAGGTTTTCC ACTCCTAGCT 660 CCTCTTGGAG GAGACCCACA CCTGACTTCA CAGGAGACGG CTCCCTTGTT CACAGGGAGT 720 GCTCTGGGGG CCAACACCGC CCTGCAGAGC TCAGCCCAAT GGGTGGCAGA CACTCACCAC 780 TGTCACAGTC ATGGTGGCTG GCGTGTCCCC AGCCAGGCAC AGCAGTAAGG GCCTTCTGGG 840 AAGTGGCTTT TTCAGCAGGA GGGAAACCCC CACTATTTCC TTTATTCAGA GCTTCAGCGC 900 CCACATGGGG TGGGGCTGAG GTTCAGTGCA GGGTGCTGTG GCTGTCTGCA CCTCCCAGGT 960 GGGATCAGAC ACTGCGAGGC AGGTTAGAAA GCCTGTGGTC TGTCCACACA GTGACCCAGA 1020 GAGCTAACAG GACCACTGAG CACGCGTCCC TCCCTGCAGC TCCCTGGTCC TCCAGCCACG 1080 GTGCCATCAG CCTGGGCCCC CACCCAGGAT CACTGACGAC CACTCCAATC TCACCCCTTT 1140 CCCCGCCAGG CTTCCCGGTG CCTCCCAGGC 1170
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