Tag | Content |
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EnhancerAtlas ID | HS104-42211 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr3:141569990-141571400 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr3:141571335-141571346 | TCCTTTGTTTT | - | 6.32 | Sox3 | MA0514.1 | chr3:141571336-141571346 | CCTTTGTTTT | + | 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 |
GH03I141851 | chr3 | 141570381 | 141570530 |
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Enhancer Sequence | CAAGTTTTTC TCCTGTCTGT TTCTGAGTAG CTGGGGTTAC AGGCATGCAC CACCACGCCC 60 GGCTAATTCT TGTATTTTCA GTAGAGACAG GGTTTTGCCA TGGTGGTCAG GCTAGTCTCG 120 AACTCCTGAC CTCAAGTGAT CTGCCCGCCT CTGCCTCCCA AAGTGCTGGG ATTACTGGTG 180 TGAGCCACCG TGCCCAGCCA TACCTGTTTC TTTTTGCATT TTTAAATATA GCTACTTGAA 240 AATTTAAAAT CACATATGTG ACTTGGCTTC CATTTCTACT GGACTGCGCT GTTCCAGGGC 300 CTTATAACAC TCCATTGCAT CCTCTCCATC TGGCTAGCAA ATAATGAGAG AGCAAGCAGA 360 GGACTGCAAA TCCCTTTGTC CAGAACTCAG TCATGAAGCC ATTGTTACAA AGGAGAAGTG 420 CATATGTAGC CTGCCCGGAA AGGAGAGGAA ACAGATTTGG TGAGCAATGA GCTGGCCTCC 480 GGCACAGGTC CAGGGTAGAA TGACAACATT GTTGGAGGTG AGGTGGTCAA GGCACTGGCA 540 GGCGGGGCAT TTGGAAAGAC TGTTTGTGAA GTCACCAAGA ATCTGAAGTG ACAGGGAATG 600 GAACTCTTCA AGGAATTCAG AGCAGTGACC CGAGTCTACA GTTGATTCAA CAAAGCTGAA 660 TATTTAGTAA ATATTCAGAT GACAGCTTCA AAGCTGAAAG CTTTGAAGAA GAGAGGAATG 720 GTGGTCTTGA AGCAGCAGTT GGGAGAAATG AGTATACCTC CTTCACCTCC AGGCCAGTGG 780 TCCAAGATGA GTAGGGGAGA GAAGAAAGGC CCCATTTGAA AGGGTGTCTG GGGAAGAAGT 840 GTCCTTATGG AGAATAGGTT TTAGTGCATG ACCTTAACCA AGTTATTTAA CCATTCTGTT 900 TGAGGTTTCC TTGGTTTAAA ATAGGGATAA GAATAACACT TATCTCATAA GGTTGTTGTA 960 TTAAATACTG AAATACAGAT GCTCCTCAAC TTATGATGGG GTTACGTTCC AATAAACTCA 1020 TGGTAAGGTG AAAATATCAT AAGTCGAAAA TGCACTTAAT ACACCTAACA TGCAGAACAT 1080 TGTAACTTAG CCTAGCCTAC CTTAAACGCA ATCAACATTC TTACATTACC TGCAGCTGAG 1140 CAACACAGTT TATGGTGTGG CTGACAGGGA CTGGCCCAGC TTGTCAAAAG AGTATCATAC 1200 TGCTTTCTAC TGAACGTATA TCACTTTCAT GCCATCTTAA AGGTGAACCA TTGTCAGGGA 1260 CCGTCTCTAC CTGCAAAATA TTTAGCATGT CGAAATGGCT ATGTTAAATA ATTTCCTGAC 1320 ATTGTACTAA AAGCACGCTG GTTTCTCCTT TGTTTTTTGT TGTTGTTGTT GTTGTTTGTT 1380 GTTGTTGTTT TTTGTTTTGA GACAGAGTCT 1410
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