Tag | Content |
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EnhancerAtlas ID | HS092-04856 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:223673310-223674520 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat6 | MA0520.1 | chr1:223674140-223674155 | GGTTTCCAGAGAAAC | + | 6.15 | ZNF263 | MA0528.1 | chr1:223674484-223674505 | TCCTCCTCCTCTCCCTCCTCC | - | 11.18 | ZNF263 | MA0528.1 | chr1:223674475-223674496 | GACTCTCCCTCCTCCTCCTCT | - | 6.16 | ZNF263 | MA0528.1 | chr1:223674481-223674502 | CCCTCCTCCTCCTCTCCCTCC | - | 6.27 | ZNF263 | MA0528.1 | chr1:223674478-223674499 | TCTCCCTCCTCCTCCTCTCCC | - | 7.21 | ZNF263 | MA0528.1 | chr1:223674493-223674514 | TCTCCCTCCTCCGCTTCCTCC | - | 7.61 | ZNF263 | MA0528.1 | chr1:223674499-223674520 | TCCTCCGCTTCCTCCTCCCCC | - | 8.07 | ZNF263 | MA0528.1 | chr1:223674496-223674517 | CCCTCCTCCGCTTCCTCCTCC | - | 9.06 |
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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 |
GH01I223499 | chr1 | 223673147 | 223674962 |
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Enhancer Sequence | GTAGCATCTG AAGCAGCCAC TGGGACCAGG CTTGCCACCC TTTCAGAGGG GTGTGAGGTG 60 CAGGGCAAAG GGTCTGTAAA GGCTGGCAGG GAAGTGGGAA GCAGTGGAGA GCCAGGACCA 120 GCCCTGGGCA CCCAGAGGGG TTAGGGACCC TGCCACCCCT CCCAGGTTTC CAAACAAGGC 180 CTGTGCCTGC CTGGGCTCTG ACAGTCAGCC AACAAACAGG CATTTCCAGG TCTGCACCAG 240 GCCCCGGGGA TACAAAGAGG AGTGAGAGTT CCTGCCCTCC CTGGATCCTG CGGGGAAGGC 300 TGACAGATAC ACCAATCCTG TGTCACGGGA ACTGGGGATT GGGGGGAATG ATGGGCAGGG 360 GGCATCAGGG TTATCTGAGA AAGCTTCCCA GAGGAGGCGG TCCCTGGCTG AATTGAAGAA 420 ATTGCTGGGA GCTTCTCAAC AAGAGCATTA GAAGGGAGTT GGGGGCACGA AGTGGGTGCT 480 CATGTCAGGA GAAAAATCCA CAAAGGCCTC TCATATGCAC TCTGCGCCCT CCTCTCATTT 540 TTCCAGGGTC CTGCTCCCAG CTGTGCAAGC TGCAAGGAAG AACGAGCCCC CTCCTCCAAG 600 GCCTCGACGG TCCACTCAGT CACCCACTTA AGAATTCACC AAATAAGTAA TGACTAAGTC 660 TGACTGGGAG AAAATGAAAG CTCTCTTGGA GGGGAAAACA AGTTACTCAT GCAACCAAGA 720 GCATATCCTT GGCACCCTCC ATGAGTGGAG CCACGGCAGG AGGGGCAGAC AGGAACAAAC 780 GGTGGCCATG AATCATGCTG TGTGCGAGCT CCTTTGTTTC TAAGGCATGT GGTTTCCAGA 840 GAAACCAGGG AACACTGCCT TCAGGTAAAC ACGCCCACCA CCCATGCTTC TTGGAACAGG 900 CTCTGTCCTC CAGGAGCCCC ATTAAAGAGG CCTAGCTGCT TACATTTGTC AGTTGTACTT 960 CCACAGGGGG GATTTCAAGT GCTAGCTGGC CAAGTCATCC AACGGGTGGC AATGGACCTT 1020 CTGTTGGCCG GGAGCATCCT ACCCCGTGCC AGGTCCCTGG TCCCACTCTG CCCACCACCC 1080 TCTCACCCCC AGAAGAAGAC TCCTCTGGTT GATGAGTTTG GCAGAAGAGT CTTGGTTTGG 1140 TCAGTTCAGC CCTTCTGCTC ATGCTGACTC TCCCTCCTCC TCCTCTCCCT CCTCCGCTTC 1200 CTCCTCCCCC 1210
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