Tag | Content |
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EnhancerAtlas ID | HS047-31689 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr7:133828480-133829300 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr7:133829030-133829040 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr7:133829030-133829040 | GGCACGTGCC | - | 6.02 | JUN | MA0488.1 | chr7:133828657-133828670 | CTGATGATGTCAT | + | 6.36 | NKX2-5 | MA0063.2 | chr7:133828987-133828997 | CTCAAGTGGT | - | 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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Enhancer Sequence | TCTGAAGCAG AAATAAACTA CCTGTGGACA GTGGTGGATG GAATAGTTTG CTATGCCCTA 60 GAGCAGTGAG TCTGTTGCTT AAATGCATGC CCAAATCACC TGTGGTTCTT GTGAAAAGGG 120 AATTCTGACC CATTAGGTCT GGGGTGGGGC CTGAGCCTGT GATTGCTAAA AACCTTCCTG 180 ATGATGTCAT GCCACTGGTC CATCGGTCAT ACTTAAGTAG CAAGGTCAGA GAGAAGTGGT 240 TCCCACACTC TTCTGCACAT TGGAATCACC TGAGGGAGTT TTCAGACCTA CTGATACCCA 300 AATCCCACTG CAAGAGATTC TGATTTAAGT GGTCCAAGGT AAGGTGTGGG CTTTGGGCTT 360 CTTATTTTCA GAGACAAGTT GGAGTGCAGT TGCGCATTCT TGTCTCACCA CAACTTCAGC 420 CTCCTGGGCT CAAGTGATCC TGTCGCCCAG GCTGGAGTGC AGTGGCGCAA TCTTGTCTCA 480 CTCTCACCGC AACCTCCGAC TCCTGGGCTC AAGTGGTCCT CTCACCTCAG CCTGAGTAGC 540 TGGGACTACA GGCACGTGCC AAAACACCTG GCTAACTTTT TTGGTATTTT TTGTAGAGGC 600 GGGGTTTCAC CATGTAGCCC AGGCTGGTCT TGAACTCCTG GACTCAAATG ATCCACCTGC 660 CTCAGCCTCC CAAAGTGCTA GGATTACAGG TGTAAGCCAC CACGCCTGGC CTGGACTTTT 720 AAAGAGACCA TCAGGTGGCT CTAATGTGCT GACAAATCTG GAAACGATCA CCCTGGGTTT 780 TGTGATTAGT GTTGTTGTAT TGGACTCAAA TATTTAATTA 820
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