Tag | Content |
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EnhancerAtlas ID | HS051-26956 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr8:145910960-145912130 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr8:145911302-145911321 | CCGCCGCCAGGGGGCACTG | + | 6.76 | KLF5 | MA0599.1 | chr8:145911414-145911424 | GCCCCGCCCC | + | 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: 1 | ID | Chromosome | Start | End |
GH08I144683 | chr8 | 145909056 | 145913579 |
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Enhancer Sequence | GGGCCTGGAG CCTCCGCCGA GGCTGGGCCA GGACCACGGG GACCGCAGCG CCGGCCCCTC 60 CGCCATCTTC TTGGCCCGCG CCGCCCACCG CCCGTTGCCC GCGCTCTCAC CGGCCGGCTG 120 CGCGCGGGCC GCGCCGCCAC AGTCCCTCAT CCCGGCCCGC GCGACGCGCG TGAGCCAGCC 180 GCCGCTCCCC GGCCTCTCTG CTGCTCCGCC GCTGCTGCCG CGGCAGCCCG TGCTGTCGGC 240 GTCCTCCGCC GCCGCCGCCG GCCCAGTGCG CGGCGGCCGC GCGTCCTCCC GTCACCAAGC 300 GCAACCCCCC GCCTCCGGCT CCGCCCCCGC GGCGGTCACT ACCCGCCGCC AGGGGGCACT 360 GCCTCGCGAG GCCGCATCAC GCATGCGCTG GCGCGCGGCA TGCCGGGAGC CGGAGTCCCG 420 CGGAGGGCGC GCGCGGCATG CTGGGAGCCG CCTGGCCCCG CCCCGTCGCC GCGCCAGAGG 480 CCTCCCGCGC GGACCTACCC TGTGAGTTAG CGGTGTCTTC CCGTCTCTTT CGGTGCAGAG 540 CAGTTACCAT CTGACACGTC TCGGTGTGGT TTGGTGTAAT TTTGCCCTCT CAAACCACGT 600 TGGGCTTCCC GAGTCTGAGA TTTCACTTTT CTTCGACTCT AGAAATACAG CCATTCTTCT 660 CAAAACGTGG GCTGCCCTGT TCCTCAGTCC TTCTTGTGGC GGGCTCGTGT CTCTTCACCT 720 CCTGTTATTC TCACCTTTTT AGTCCTGTCA CTTTTACTCG GTAATTCACT CAGCTGCAGC 780 TCGACTAGTG CTCTATTCGG CGTTTTCTAA TCTGCGTTCA GCCTGGTTTT CTAGATTCTC 840 TTAGTGCCAG GTGCGTTTCT GGAAATTGAA TCTGACTGGC ATTTCTGGAG AAACGGAGGC 900 TAAACAGCCT GAAGCTTCGA TAGTAGAAGA CAGGGGCGCA CACCCTTCAG TCCTGGACAT 960 TCCCTGGGTC CTCAACTGTG AGAAGCCGCA AAGGGCTGAA AGGCCCCCGT CAAAAGTCAT 1020 CCGTGGAGCT CCACCTCCTG CCCTGCAGCT CAGTCGCCTT GCAGGGACTC TCCCGCCTCA 1080 GGAGATCTCC CGTCGGGCTG TCTCGCCGCC CGCGCTTCCC TGTTGGGCCG TCGTCACACT 1140 TCACTCTTCA CTCTTATACA CAGGGCTCTG 1170
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