Tag | Content |
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EnhancerAtlas ID | HS118-02049 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr10:11878860-11879700 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr10:11878889-11878902 | GAAAATTCCAGAA | - | 6.17 | TBX20 | MA0689.1 | chr10:11879276-11879287 | AAGGTGTGAAG | + | 6.32 | TBX21 | MA0690.1 | chr10:11879276-11879286 | AAGGTGTGAA | + | 6.02 | ZEB1 | MA0103.3 | chr10:11879009-11879020 | CCCACCTGCCC | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGTCAACCGT GGTCCAAAAA TATGCGATGG AAAATTCCAG AAATAAATCC TTCATAAGTT 60 TTAAATTGTG CACCATTCTG AGTAGTGGGA TGAAATGCGT CGTTCTGATC CATTGCCTCC 120 TGCATGCGAA TCCTCCTTTG CCCGGAGTCC CCACCTGCCC ATCACTTAGT AGCCAACTCA 180 GTTCTCAGAT CAGCTGTCTA TGTGGCCGTG CTTATGTTCA AGTCACTTTT ATTTAATAAT 240 GGCCCTGAAG CAGAAGAGGC ATGATGCTGG CTGGTAATTT GTATATGCTG AAGAGAAGCT 300 ACCAAGTGCT TCCTTTAAGT GAAAAGATGT GAAAGTTCTG AACTTGGAGA AGAAAAAAAA 360 ATCAAATGCT GAGGTCGCTG AGACCTACTG TAAGAACAAA TCATCTTCTG TCTGTGAAGG 420 TGTGAAGAAG GAAAAAGAAA TTTATATTAG TTTTGCTGTC ACACTTCATA CGTTCAAGTT 480 ATGACCACTG TGTGACAAGT GCTTAGGGAC ATTTGTAGGT AGAAGACATG AACACGAGCT 540 CCGATTGCTG GCAGACGGGT TGGGATTGGT GCTGTCTGCA GATCCAAGCA TCCACTGAGG 600 GTCTTGGAAC ATACCCCCTC AGAGAAGGGA GAACTGCAGC AATATAGGTA CATGGGGTTG 660 TCTTCAGACC CAGCCTGGAC CTGTTTTTGT GAAGTGTTTG CAATGGCAAT GAGTTGCGTA 720 ACATAGACAT ACTAAGCAAG ATTGGTTCTA CATCACTTGG TTAAGGGGAA TAATTTTTCC 780 ATTCACGTTC AGAACTACCA AAGACAGTAA TGACCTTGTG ATTTGGTTGA AGCTGTCTGT 840
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