Tag | Content |
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EnhancerAtlas ID | HS165-14856 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr8:10822340-10824010 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr8:10822798-10822808 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr8:10822798-10822808 | GGCACGTGCC | - | 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 |
GH08I010965 | chr8 | 10823160 | 10823372 |
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Enhancer Sequence | GCAGCATCCT CTAAAGCCCT TTCCCCTGAC ATAGCCCACG TCTGTGAGAA CTGCATTCGG 60 ACTTAGTTTC CCCGGCCAGC GCTCCAGGGC GCTGTTAAAC CCAGAATCCA CATCCCCGTG 120 CAGGTGTGTT TACAGGCTTC CTCCACTAGG GATCCAACCC TCCTCTTTAC ATCGCCTTCC 180 CTTTCCTCTC TCTTAAAGGG ACAGGCCAAG GGCCACCAAC TGGACTGGAC CACAAGCCTG 240 CTTGTTGGGC TCTCAGCTTA GGAAACCATA TTGCCAAGGC CCCAGAACCT GAACACCAGC 300 AAGCTCTGGC CTCATGGATG GCGGGTCCCC TGGGTCCTGT GGACACACGT CCTTCTTAAG 360 TCCTTCCTTG CCAGTTCTGA GAAAGCCCAT TTCCTTCCCA GTTCGGCTCA TCTGAGCTCT 420 GGCAAGCACA TCAGCCCTAC GGGCATGGAT GCAAGCAGGG CACGTGCCCT CGATCCTCTC 480 ACTACAGAGA TGCGGGAGCA ACGGTGGAAG GCTCCTCCGA GCACCACGGT CCCCCAGGGA 540 TCTGGGGGCC CCACAGACTT TCCCACTCAA GACACAGCCT AGAGGCAGCT GTCTGCCTGG 600 TTTGCTGCTG ACTGCTGCAC CTAGCATGGC ACCTCGTGCG CAGAGAACAT TTTGCTGCAT 660 AAATGCAGGG AGGAGGAACA CAAGAACATT CTCGGTACAT ACTCATCGTA CATGAGCTGC 720 TAAGGCACGC AGGGGGCCTG TGGGACGGGC TCCCGATTCC CCTCTTTCCA GACAGAAAAC 780 CAAGGCACCA AACAGCTCGC TTGAGACTTG GGAGAATGAA GGCTTGGTGC CCGGAAGCGC 840 CATCTCTCTC TTTCCGGCAG CTGCAGGGTG TTACCGGGGC AACAGACGGC TGTCTGACGG 900 GATTTGGCAG TTTAACTCTT ACTCCGCACA AAATACGAAA GTGAGAACGA TTGAACAGAT 960 GTTCTTGCTT CCGACCGTTC ACACAACGGA GAGGAGCTCA TGATTCATCT GGCCCGGGCC 1020 GAGTCCACAT CATTCCTGTC TCACACCCAG CAGGTGTGGG CCACCTGGTC CCCTGGGAAC 1080 CAAAAAACGG CCTTCAACCT CCCAAACTCT AGGATTCCTC AAGGGCATCA AATTCACCTT 1140 CCAGCCTGGG CTGAGAAGAC TGAGCTGGGA TCCTTCTGAG GTGCAACCAT GCCAGGCCTA 1200 GAGCAGCGGT TCTCAAACCT CGGGTACATC CAGATAACTT GGGTGGGGAG GAGGATTGCT 1260 AAAACACAGC AACCGTGCCA GGTGCACAGC AGCGGTTCTC AAACCTCGGG TACATCCGGA 1320 CTACTTGAGT GGGAGGATTG CTGAAACACT GACTAAGAAA CACAGAGTTT CTCATTCAGT 1380 ATGTCGAGGG TAGGGCCCAG GAATTTCCAT TTCTAACAAG TTCCCAAGTG ATGCTGATGC 1440 CGCTGGTCCA TGGACCACCC TTGGGAGCCA CTGGTGTATA CAGCCTTCCC ACTCAGAACA 1500 CAGTGCCTGT ACCATCACCA TTAGCATCAC CGAGAAATGT ATTAAAAACG CAAGTTAGGC 1560 CGGGCATGGT GGCTCACGCC TGTAATCCCA GCACTTTGGG AGGCCAAGGC AGGCGGGCGG 1620 ATCACGAGGT CAGGAGATCG AGACCATCCT AGCCAACATG GTGAAACCCC 1670
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