Tag | Content |
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EnhancerAtlas ID | HS092-07575 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr10:104276900-104278160 |
Target genes | Number: 24 | Name | Ensembl ID |
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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) |
Foxd3 | MA0041.1 | chr10:104277062-104277074 | AAACAAACAAAC | - | 6.32 | HNF4G | MA0484.1 | chr10:104277374-104277389 | TGGCCTTTGGCCCTT | - | 6.88 | SOX10 | MA0442.2 | chr10:104277051-104277062 | AAAACAAAGCA | + | 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 |
GH10I102517 | chr10 | 104277041 | 104277840 |
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Enhancer Sequence | TGGGCATGGT GGCACACACC TGTAAACCAA GCTACTTGGG AGGCTGAGGC AGGAGAATCG 60 CTTGGACTCG GGGGCCAGAG ATTACACTGA GCCGAGATCT CGCCACTGCA CTCCAGTCTG 120 GGTTAAGGAG TGAGACTCTG TCCAAAAAAA CAAAACAAAG CAAAACAAAC AAACAAAAAG 180 AACAACTGAG TGGTGTGGTA TTGTAAGTGA CTACCAGGCC AGAGTGGTGC CAGGTAGGTC 240 AGCGCTGGGA AAGTTCCTTC TCTTCCTCAA GAGACTTGGA AGCCTTTATG GGTTTGATGC 300 AATCTGATCT CTCAGTCCCG GGATTTTTCC CTGTTCAGCC CACCCTTTTG GGCTCTCCTC 360 TTCCAAGCTG TGCTGTTATC TATTTTGAAT GCTATTCCCC ATACCTCTCA TGTCCTGGGT 420 CTGAGTTTGC TAGCCTCTCC CTTATCCACC TTTCTGATTC AGGGGTCCCA ACTCTGGCCT 480 TTGGCCCTTG ACTCCTGAAT TCATTCATGT ATCTTGCCTC TGAGGTATTC AGTGCAGCTT 540 CATTTCTTGT TTCAGTTCTG ATGTTGTTCC TGAGATGTGT CTGGTGGGAT CTTATCCTCT 600 ATGACCTCAG CCCTGAGGAA TGGTATCCTC ACCCGTCCAA CTAACTTTGC AGCTTGCTGT 660 CCTGCCTACC AAGCTCTTGA GAACCAGGCT GTGCAGCACA CTCACCAGCA GAGCTATCTT 720 GAGTCCCCTG TACAGGCAGA ACATTGGACA AGATGATGTG TTTGAGTGTG GAGACAATGA 780 AGAATCTGAC CGAGCGCCTG CCCTTAAAAA TGCAGCATGT GCTTGGTAGG AGATGGTGAG 840 GTCCTTGAGA AAGAAGATGA CAGTGAGGAT TGGGACTGGG AGCAGCTTCC TGTCTCCCTG 900 TGACTTTGAG GCTCTCTCCC CTCATCCTGT GATCTTCAGT GTTCCAAGAA ACTTTAAACA 960 TATAATTATT ATTACAAACA ATTATAGCCC TTACTTTGTA TAAGGCACTT TTCTAAGTGC 1020 TTTATATAAA CTCATTTAAT CCTCAGAACA ACTCTATGGT GTAGGACTTA TTATCCTTAT 1080 TTTACACATA AGGAAACTGA GATGCAGAAA TGTTAAGGAA CTCATCCACC CAGCCAGTGA 1140 ATGCTGGAAC TGGGATATAA ACCCAGGCAG TCTGGATCCA GTAGTCACCA CCTCCTTTTT 1200 CTACCTCCTG CAGAGAGCTG GAGAATTCTA TTCAGAATTA TGCTGCTAAA TTCAAAGTTA 1260
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