Tag | Content |
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EnhancerAtlas ID | HS188-10268 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chr5:75476200-75478070 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr5:75477067-75477079 | ATCTGTTTACAT | - | 6.62 | FOXP2 | MA0593.1 | chr5:75477068-75477079 | TCTGTTTACAT | - | 6.02 | NFE2L1 | MA0089.2 | chr5:75477111-75477126 | AGAGCTGAGTCATTG | - | 6.17 | POU2F2 | MA0507.1 | chr5:75477987-75478000 | TTGATTTGCATGT | + | 6.12 | ZNF263 | MA0528.1 | chr5:75477411-75477432 | GGTGGAGCAGGAGAGAGAGGG | + | 6.68 | ZNF263 | MA0528.1 | chr5:75477414-75477435 | GGAGCAGGAGAGAGAGGGAAG | + | 7.15 |
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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 |
GH05I076180 | chr5 | 75476265 | 75478186 |
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Enhancer Sequence | ACAAGACACA TAGTAGCACT TTTCTTCCAA AATAGCCCAC TCTTCCAATA GCATAAGCCC 60 TTTGCTATAG TCTATTACAT CTGCGGCTGT GGTTTCAAGG CAATCATGTC CATATTAATA 120 TACTTGATGC TTTTCTTCTG TCTTCACTGA TGCCCTGTGC TGACGCATTT GTTCCAGTTC 180 TTTTCAGTCC AGTGACATGG TACCCTCTTG CTCCTCTGAA TTGCAGTTGT ACTTAGCTAC 240 ATCCCTGGCC TCCTCCTCTC ACTGCCCCCT CTGCTTTCAT CTCCTGTTCT CTGCCTTCGT 300 CATTCCTCCT GGCCCGAGAC TGCCCCTTCA ACCTTGCCAG TGACCTCTTC CAGGACGGGC 360 CCAAAGGTCT TTTCTGAGCT CTCATGCTGT GGACACTGTT GAGCAGCCTT TCCTCTTCAG 420 TTTTTCTTCT GAGGTCTTCT CTGCTCTATC CAGACCCTTC TTCTTATTTC CTTGTCCACA 480 CTTTCTTACC TCTGACTTCT TTTCCTTCTT GCCGTCTAAA TGTCACCATC CTCAAGGGTT 540 GACTCTTTCA CTTCTTCTTG GCCATATCCT TTGAGCCTGG GTCATATCCT TTCACTTACT 600 CTTGCAGGGA AATCACATTT CGCAAGGCTC TCAACTGCCC TGCTATGCTG CCACCTCCCA 660 AGTATGTTTC TTCATTTCCT TACCCCAGCC TTGGTGTTAC ACTTTCCATT GCCTCTCAGC 720 CATCCCCCTA CCTGTTCAAT TAATACACAC CTACCCTCAG GCAAACGCTT CCTCTAAAGC 780 AGGAGTCCAT AAATGACAAC CAACAGCTCC GATCCAACCC TCTGCCTGAT TCTGTAGATA 840 AAGGTTGGTA GGAACACAAC CACACCCATC TGTTTACATG TTGTCTATGG CTGGTTCCAT 900 GCCGCAGCAG CAGAGCTGAG TCATTGCAGT AGAGTCCGTA TGGCCCACAG AGTCTGAGGT 960 ATTTACTATC TGGCCTTTTA CAGAAAGTCT GCCAGTCCTG TTCTACAGTG CCTTTGCCTT 1020 TTCACACTAG GGCTTTCTAT TAGTCTGTTT TCACACTGCT ATAAAGACCT ACCCGAGACT 1080 GGGTAATTTA TGAAGAAAAG AGTTTTAACT GACTCATAGT TTCACAAGCT TAACAGGAAG 1140 CATGGCTAGG AGGCCTTGGG AAATTTACAA TCTTGGCAGA AGGTGAAGGG CAAGCAAGCA 1200 TGTCTTACCA TGGTGGAGCA GGAGAGAGAG GGAAGGGGGG ATGTGCTGCA CTTTTAAACC 1260 ATCAGATCTC GTGAGAACTC TGTGAGGAGA CAGCACTAGG GGGATAGGGC TAAACCATTA 1320 GAAACCACCC CCATGATCAA CCACTTCCCA CCAGGCCCCA CCTTCAACAT GTGGGGATTA 1380 CAATTCAACT TGAGATTTGG GTGGGGACAA ACAGCCAAAC AATATCAGGC TTTGATTGCT 1440 TTCCTTCCCC ACGCAGGAAC CCATAAGTGA CTCCTCATTG TCTGTATAAG TAATTTAAAT 1500 GCTTTTGCTT TGATATTTAG GAGTCTTCTC ATACTCATCC AGCCCAATTA TATTTCTCCA 1560 CACACTAAAC CCAGTCATTC CCACCAGACA CCTATCCTCC TGACCTTTCC AACCTTCTCA 1620 TGCCTCCTAC GTTAGACCTT CTCCAGGACT GTTGTGTAGT CCTGAAAGAA AGCAAAAATG 1680 CCATTCCACC TATCCTCTCA TTGTTCATAT TCTCCTTGGT TTTTATTTTT ATTTTTTGAA 1740 GCTCCTGAAT CATTTCCTGA TGGTCAGCTG TATTGACCAC TGCTTTATTG ATTTGCATGT 1800 GTTGCCTGCT CTGCCCTATC CTGCCCTGTT CACATAGAGT AGAATGAGGG TTTCTGTTGT 1860 GAACATCTTC 1870
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