Tag | Content |
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EnhancerAtlas ID | HS183-01425 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr12:133169640-133171300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF14 | MA0740.1 | chr12:133170736-133170750 | AGGTGGGCGTGGCA | - | 7.14 | SP3 | MA0746.2 | chr12:133170737-133170750 | GGTGGGCGTGGCA | - | 7.12 | SP4 | MA0685.1 | chr12:133170735-133170752 | AAGGTGGGCGTGGCAAC | - | 6.33 | SP8 | MA0747.1 | chr12:133170737-133170749 | GGTGGGCGTGGC | - | 6.62 | ZNF263 | MA0528.1 | chr12:133170577-133170598 | GAAGGAAGAGGAAATGGGAAA | + | 6.12 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 133170084 | 133170319 | chr12 | 133170352 | 133171030 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I132593 | chr12 | 133170057 | 133171053 |
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Enhancer Sequence | TTGAGCTGAA ATTCACATCA CATAAAATGA ACCGTTTTAA AGCGTACAAT TCGGTAGCAT 60 TTAGTCCATT TGCGATGTTG AGTGACCCTC ACTCCCGTCT GGTTCCAAAC GCTCTCCACC 120 TGGAAGAGAA CTCCCTCCCC GTGAGCATCT CTCCCACCGC CGCCCTGGCA ACCCGGGCCT 180 CCTCCCGCCT CCGGACCCGC CTGTTCTGGG CCTGCATAGA AACGGAAGCT CACAGTCGGG 240 GCTGTGTGTC TGGCTTCTGT CCCCCATCGC CATTCTCCAG GCTCACCCCC TGCAGCCGTG 300 CGGGCCTCAT TCTTTTCCTG GTGGAATCCT GTTCCCTGGT GTGGAGGGCC ACGCTGGGCT 360 TATCTGTCGA TCGTTTGTGG ACACCTGAGC AGCTATGAAG AGTCTGCTTT GAACATCTGT 420 GGACAACAAT TTGTGTGACG TCTGTTTCCG ATTCTCTTGG GTTTGTCCCA GGAGTGAGCT 480 TTGGGGTCAG ATGTCCAAGT TCACAGTCAC ACTCGAGCCG TGACCTCGGC CGGGGCCTTG 540 CCAGGTCCAG TCCTGGCCTC AAGATGCCCC TTCAGGGTCA GCCCGCAGCC AGGGGTCCCA 600 GAGCAGGCAA GGGCTTGAGG AGGGCCTCCC GGGGCTGGGG CACCTGCCTT TCAGGTGAAA 660 TATCAGAGTG TTCAACCCAG ACCATACCAA TGGCACCCGC GCGGAGTGCA GTCACCAGGG 720 AACCGCCCTG CGGCGATGGC CCCGGCGGGG AGAGGGTGGG TGACGTGCGC TGCGGAGCAT 780 CTGCCCTGGT GGAGGTGCAG CCCCACTCAA AAAGGTTCAC CGTGTGAGTT AAAGATGTTT 840 ACTGTGAACC CTGAAGCAAC CACTAAAACA ACAAAACAAA ATTCTGGCTC ATAAGCCAAC 900 AACTGCAATC AAACAGGATC ATCAAACAGA ATCCAAGGAA GGAAGAGGAA ATGGGAAAGG 960 GAGAGCCGGT GACAGCAGCG GGAGCAGAGA GCAGGACGGC GGGCGTGGCC TCTACACAGT 1020 GAGACCAATG GGAGCAGAGA ACAGGATGGC AGGCGTGGCC TCTGCATAGT GAGACCAAAG 1080 GGAGCAGAGA ACAGGAAGGT GGGCGTGGCA ACTGCACACT GAGACCAATG GGAACAGAGC 1140 AGGACAGCAG GCGTGGCCTC CACGCAGCCA CAGCCACACC GGAGCAAGTG GTCAGACAGC 1200 CCCAGTTAAG AGCAGAGATT GCCAGGGAGG GTAGGACAGC AAAACCCAAC GCTAAACTGC 1260 TCATGAGAAA TGCACTTTAG ATATGGACAC CAATAAGTCA AAAGGACAGG AAAAGCTATG 1320 CCATGCAAAC AAAAATTTTT AAAACCTGCA GTGACTATGT CAATATCAAA GTAACTTCAG 1380 GGGCCGAGCA CGGTGGCTCA CGCCTGTAAT CCCAACACTT TGGGAAGCTG AGGCGGGCAG 1440 ATGACTTGAG GTCAGGAGTT CGAGTCCAGC CTGGCCAACA TGGCGAAACC CTATCTCTAC 1500 GAAAAATACA AAAAGTAGCT GGGCATGGTG GTGGGCGCCT GTAATCCCAG CTACTTGGGA 1560 GGCTGAGGCA GGAGAATCAC TTGAACCTGG GAAACAGAGG TTGCAGTGAG CCGAGATCGT 1620 GCCACTGCAC TCCAGCCTGG GCAACAGAGC GAGACCTTGT 1660
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