Tag | Content |
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EnhancerAtlas ID | HS030-14997 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr8:9160230-9161690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata4 | MA0482.1 | chr8:9160901-9160912 | AGGAGATAAGA | - | 6.14 | TEAD1 | MA0090.2 | chr8:9160805-9160815 | ATGGAATGTG | - | 6.02 |
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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: 2 | ID | Chromosome | Start | End |
GH08I009302 | chr8 | 9160243 | 9161355 | GH08I009304 | chr8 | 9161521 | 9161670 |
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Enhancer Sequence | TACTAAAAGA GCTATAACCC TTTCAAGAGA AAACTGAGGT CAGATTTCTT GCTAACCACC 60 TCTTACAGGG CAATTTGATG AGCAAGGTGT GTATTGATTC AACAGCACAG GAGGCCTTGC 120 TGTGTATTGG TAGCACTGCA AGTGCCAAAG GCTCAAGGAA GAACAAGGAA AGAGCTGAGA 180 AGGTAAATCG CTGGCATTTT GTAGGCAGGG ATAGAGAGAC TAGAAGAGTG GGAGGATTGA 240 GGATACTGGA AAAAAATGGC TAAAGTGGTG CACTAGGGAG AGAAAAGGAA GGAAAAGGCG 300 GGTAAGAGCC AGGTATAGGG GAAGCAAAAT CCGTGGGCCA TGTGAGGAAG AAAGATAAAG 360 AATTTGGCAA TCAAAGTCAC TTAGTGCAGT GCTTCTCTAA CTTCAGTGTG CACACGAATC 420 ATCTGGGGAT CTTGTGAAAA TTCAGGTTCT GATTTAGCAG GTCTAGGGCC AGGCCTGCAA 480 TTCTGTATTC CTCCCAAGCT CCCAGAAGAT GCCCGAGCAG GTGCTGGTCC AGCCCACCCA 540 TGAGTAGCAA GACCAGAGGA TCCCAGTTTC ATCTGATGGA ATGTGAAGAA TGTCAGTACC 600 AATGAGTGAA TTCCTTATTG TCAGTTGTGT ACTTTGCACT CTGCTAAGTA CCCTGAAGAG 660 TTTTTAAAAA GAGGAGATAA GACATGCAAA CATGAAACCA CTAGAGTAAA ACAGAAGAGT 720 GTGTGCGTTA CGGAGCCTAC GTGGGGCTGG AAGTCTTCGG GAACAGAGAG GATCTGTCTA 780 AGCATGTTGG AGCTTACACA GGCAGAAAGG AGGGGGAGTG GCGTCAAGCT GAAATGAACA 840 TAGAGGGGTA GAGTATGGAA TGCCAGTGCC GAAGAACTGC GGAGACCTCT GTGGGGTCTT 900 AAAGCTCCAC TGCAACCCCA GAAAGTGACC ATCTCTAGAG TTGAAAGGCT AAGTGTTGTG 960 GTGGCTGGCT GAGTTTAGCT GAAAAGGCAG GTGTGTCTCC TTTAGTCTTT TCTTTCTTTT 1020 CTTTTTTTAG AGACAGGGTC TTGTTCTGTC ACCCAGGCTG GAGTACAGTG GTGCAGTCAT 1080 AGCTCACTGC AGCTTTGAAC TCCTGGACTC AAGCAATCCT CTCACCCCAG CCTCCCGAGT 1140 AGCTGGGACC ACAGGCACAC TTCCACCATG CCCAGCTAAG TTTTTTATTT TTTGTAGCCA 1200 TGGGGGGGGT CTCATTATGT TGCCCAGGCT GGTCTCGAAC TCCTGGCCTC AAGTAATCCT 1260 CCTGCCTCAG CCTCCTGAAA TGCTGGGATT AGAGGCATTA GCTATCACAC TCAGCCTCAT 1320 TCAGTCTCCA GAGCACCTGG CACATTGCTG GACACATTAA TGGCCACTGA GGAAGTGGCT 1380 GACTCATGCC AGGGCCATTC AATGAATCAC GGAGCAGCCA GCATGCATAG TAACTAATAC 1440 ACCTTAACAT CGAGGTTCAA 1460
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