Tag | Content |
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EnhancerAtlas ID | HS183-13777 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr9:131105570-131107430 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Sox3 | MA0514.1 | chr9:131106812-131106822 | AAAACAAAGG | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGTGAGTAC CTGGCCCAGC CTTTCCTGGG GTCTGCCACA CTACAGTGAG CTTCTGGTCC 60 CCCAAATCTC CCCAGGCCAG ACCTCATGTT CTCTACCAGC ACAGGGCAGC TGAGCTGAGT 120 TCCAGAACAG CAGCCTCTGC TCCACACCCG TACCCTGGCA ATAGTACCTG GTCCCTCCAT 180 CTCCAAGGTC AAAGTCTTCT CCCAGGGAAT CTCCCTAACT TGAGGCTCCC AGGCCTTGGG 240 CAGGCTTGGC CTAGGACGTA CATTGAACAC CAAGTGTGTT GAGACATCTG CAAGGGGTCC 300 TGAGGACTCT GTAAGTTTAT GAAAGGGTAA AGAGGAATTT TGGGGAAAGG CCCTGCCCTC 360 AGGTTGGCAG GGGTGTGAGA TGGCACAGGG GGCACTGAGT TCTAGAGCAG AGCCCCTACT 420 CAGATGTCTG GGATAACCTG CTCCCCAAAG AAAGCCCGGT ATGCTCCAAG GGACATCCTG 480 TACCAGAAAT ATCTATTCCC GCTTGTTCTC TACTAGGTGC CAGGCTAGCT TTGGGGTCCA 540 GAGAGGAATA AGGCAGACCC CATCTGCCAA GCTCAGATTG GTCAGGAGAA AGAAAGGGAC 600 ACAGCACATC TGTAAATTGG CAGTGCCATG TGGGCAGAGA CCCTGGCACA GCCTTGCTCA 660 CTACTGTGTC CCAGCACCCA GTTCAGTGAC CCACACCCCA CACAGGCAGC TCAGCATTTG 720 TCAATCTTGG TTGATTGCAA AAGAAGGCAC GGAGTGGCAC ACCAGGAAGG GTGGTAGCTG 780 TGGGAGCATG GAGCAAGGAG AAACAGCTGC CAGCCAGGAC CCTGGGAATC AGAGAAGGCC 840 TCCTGGAGAA AAAGCGGCTG TACTTGAGAG GCGCCTTAGT GGTGGTGGAA GGAGATGAAT 900 CCAACCAGAA GGCACAGCAT CAGCAACAAA GGCATGGAGT CCAGGGCTGG GCGCAGTGGC 960 TCACACCTGT GATCCTAGCA CTTTGGGAGG CCGAAGTGGG TGGATCACTT GACCTCAGGA 1020 GTTTGAGACT AACCTGGGCA ACATGGCAAA ACCCCGTCCC TACCAAAATA CAAAAAAGTT 1080 AGCCAGGCAT GGTGGTGCAC ACCTGTGGTT CCAGCTACTT GGGAGGCTGA GGTGGGAGCA 1140 TCATTTGAGC CTGGGAAGTG GAGGTTGCAA TGAGCTGACA TTGCATCACT GCACTCCAAC 1200 CTGGGTGACA GAGTGTGACG CCATCTCAAA AAAAAAAACA AAAAAACAAA GGTGGCAGGA 1260 ATGGGATGTT GCCAAGTGAT TCCACAAACT TATTGAACAT CTACTCTGCC TGGCACAGGA 1320 CCCAGGGGAT AGAGTGTTGA ATAAGACAGA AGCCTATCCC AGCTAGGCTC ACAGGGAGGA 1380 AGACTGGACA GACCAGCAAA CTCATTCATT ATTTACTGTG GTCATGGTGG GTCGAGGGAG 1440 CAGCTGGACT GTGGGAGGCC CCAAACAAGG AGTTTGGACT TTTACAGGAA GCTCTGGAGA 1500 CCTAGGAGGT TTCTGCTGGA GCAGCAGGCT GAGAGGGTAG GAGTAGAACT CTGGAGCCAG 1560 AGAGGCCTAG AGTTCAAATC TCAGCTCAGC CACCCTCCAT CCATGAAGCT TTGAGCAGGC 1620 CACGGCACCA CGAGAGCCTT GATTTCCTTC TGTGTAAGGG GAGGGGAATC ATACGAACTC 1680 TCAGTGTTAT TGAGAGGCAT CAGTAAGGCA GTGCATGTTC CCAGCAGGAG CCAGGAGATA 1740 GAAGTGTTGT AGGGGGTCTG GCTCATGAAG CATAGGCTGG CGAGGCAGCA GCCTGGGGTA 1800 GGGTGTCAGG ACCCCTCCCT CCCAACCATG GCAGACACAG CGCCCTCTCT TGTTCACACA 1860
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