Tag | Content |
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EnhancerAtlas ID | HS050-65331 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr8:26297270-26299220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr8:26297783-26297794 | AAAACAAAGAA | + | 6.62 | ZNF263 | MA0528.1 | chr8:26298556-26298577 | CCCTCCTCTGCCTCCTGCTCT | - | 6.58 |
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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 |
GH08I026436 | chr8 | 26294140 | 26300315 |
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Enhancer Sequence | AGACTTTCAC TAGGTCCTTG TAGGTGGAAC CTTAGTGGTC ACAGTGGGCC AGGAGGGTTT 60 GGCTAGTTTT GGCCTTTGTA GCCATCTTTG AATTACACTA TTAGTAGATC AGTCTGGTCT 120 CTAAAAGGAA AAAGACCACA GTCATTATTG GAGTTTGACT ATTCCGTTTA AAATGTAGCT 180 TTTAAGTGAG GTACATCATA AAGGATCTAC TGGCTGGGCA CGGTGGCTCA CGCCTGTAAG 240 CCCAGCACTT TGGGAGGCCG AGACGGGCAG ATCACTTGAG GCCAGGAGTT TGAGACCAGC 300 CTGGGCAACA TGGTGAAACC CCATCTCTAC TAAAAATACA AAAATTAGCT GGGCATGGTG 360 GTACGTGCCT GTAATCCCAG CTACTCAGGA GGCTGAGGCA GGACAATCAC TTGAACCCGG 420 GAGGCGGAGG TTTCAGTGAG CCAAGATCAC TCCATTGCAT TCCAGCCTGA GTGACAGAGC 480 AAGACTCTGT TTAAAAAAGA CAACGAAAAC CGAAAAACAA AGAACAGGTG GAGTCTACTG 540 ACTTGCATGA GTCAGGTAAT TCATTGACCG GGGCTGGTCA AAAAGATGGG TTGATCCTTA 600 CTGTGGAAGC TCTCAGCTGC CCTGCAATAC TTTGGAAATA AACCAGGCAA AACACTGCTC 660 AGTGTGCTGC ACTCCAGACA CAAACAGGAA GCTGCTCTTT CTCTGCTTCC CTCCCCCACA 720 ATCAGACTCT TGTAACTCTC TTTTCTTCTT TTTCTAAAAT GAATCTGGGA GTTTCCTTTA 780 GCCCCTGTTT TGTGGTCGCC TCCCATACAC GTTTTATCTG TCCGTGGCAT TTTCTTTTAT 840 TTATTGAAAG CACCGTGTCT TAGATCAAGT CTTGAGAAAC AGAACCTGAG ACAAACATGA 900 ATGTGGTTAA TTGAACGAGC GCTGTGCAGG AAAAGCTGTA CTGGAGAGAG GTAAGCGGAC 960 AGATACGGGG AAGAGCTGGG CCCAGCAAAG ATGAGGTCTC AAGTAAAGCT TATGTTTGGC 1020 TTAATCCACC GGGGACGGTT CTGGAACATA AGCCACACCG CAGAGCTGTG ATGTCACACC 1080 TTGAGGCGAG GGCCTTGCCT CCTGGTATCA GTCAGTCCTG GCTGTGGGGA GCAAGGTGGC 1140 TCCACTCAGT GCAAGGCCAT CCTGGGCAAG GGGCAGCCCC CCTCACCGCA GTGGCCTGGC 1200 AGTGGGGCCC TGGGTCCGGC ACAGCTCCTC CTTCGCACAG TGCTGTCTGC TCGCCCGGTG 1260 TCTTTCATGC CGTTTCCCAC CAACTTCCCT CCTCTGCCTC CTGCTCTGCA TTGCACAGTG 1320 CAGCGAGGTT GCCAATTCCA TAGTTGTAGC GGCTGTGGGG GAAGGGGCAG GCGGGACAGG 1380 GGAGGCAGCC ATCTAACTTT TGTCCTGACT CACGCAGGCC TGGCCTGGTG TTCAGAACAC 1440 AAATGTGAAA AATCAGACCG GGAAGATCAC GGGAGGCAGG AAGCATCTGG TTTGCAGGTA 1500 GGGAAGTGAC AGACCCCGCG GATGCCATGC ACAAGGGTAC ACAGTGGAGT GGGGATGAAA 1560 TCAGGGCGGA AGTGCAGGGC TCCTGAGCCC GGGGCTGGGG CTGTTTCCCC AACTGTCCGC 1620 TGCCTCTGCT GCCTCCTGAG ATCGTCTCCT TCTGCTGTCT GCCCGCTGGA ACTTATTTTT 1680 AGTTTTAATT TTTTCGAGAC AGGGTTTTAA TCTGTCACCT GGGCTGGAGT GTAGTGTCGT 1740 GATCAGGGCT GACTGCAGCT TCAACCTCTC GGGCTCAAGT GATCCTCCCA CCTTAGTTTC 1800 CCAAACAACC AGGACTACAG ATGCATGCCA CCAAGCCTGC CTAATTTATT TTTTTATTTT 1860 TCAATTTTTA GTAGAAATTT AAAAATCCCC CAGTGTGGCT GATTGGCTGA CAGCCACACT 1920 GAAGCTTTAT TCCTGCCTCT CCTCACTCAG 1950
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