| Tag | Content |
|---|
EnhancerAtlas ID | HS047-26538 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr5:1827570-1828720 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr5:1827980-1827991 | GCTTCCCGCCC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH05I001827 | chr5 | 1827743 | 1828695 |
| Enhancer Sequence | AGGACTTTGA AGGCACGGGG GCCACGCCTG GCATCCCCTG CCCCATCACG CTCCTCGCGT 60
GGAGCTCTGT TTCCCAGCTT GACTTTGTGC CTAGATGAAC CGGCTGAAGG ATGCGTGACT 120
TGACTGCGTA GATGAACCGG CTGGTAGCAC ACTGCGGCTC CTCTTATGGA AACATGCTCC 180
TGGCCCTGTG GCCTGTGGGG CCCCCCCTCC CCGGATGTTC GCATCATCTC GCCAGGTCAG 240
CTCAGCAATG TCGTCTAACA GCCGGGACTG ATGTGGTCTG CATGGCTGAG CCCCCCAGAT 300
CCGAGTGTTG AAACCCTCGG TGGGGTTATG AGGAGGCGGG TATGAAGTGG TATGAGGAGG 360
AGGGTCCCTC AGGAATGGGA TTCGTGCCCT TATAAAAGGG ACTCCAGAGA GCTTCCCGCC 420
CCTTCCACAA AGTGAGGACA CAGCGAGAAG GGGCTGTCCG TGAACTCGGA GCTCTCAGGG 480
GACACGAAAC CTGCCGGAGG CCTGATCCTG CGTGTCCTGG GGCTCTCCGT GGGCATTTCC 540
TGTCTGCGTG GAGAGGCACA GCCGCAGCGG GAGCCGGAGC AGGTGGTGTG CAGGGAGAGG 600
CGGAGCCGCG CGCAGGGAGG GGCGGAGCCG CGCGCAGGGA GGGGCGGAGC CGCGCGCTGG 660
GAGGGGCGGA GCCGCGCGCT GGGAGGGGCG GAGCCGTGTG CAGGAATGAG AGGGGCGGGA 720
GAGCCCGATT TCACTGCTTG CGCCCTTGGA TGCTGCTTGA GCCCGGTTGT GGGTTCTCAT 780
TCTGTTAGGC AGATTGGGCT TGGTGTTTAT CCCATTCACT GGATGGAATC CTGGTGGACT 840
GAGGTCTGGC CCCCGCTTAG GAATGCGGAG ATGGGAGCAG GTTAGTCCTG TGCTGGCTCC 900
GAGGTCGCCC TGAGGTCGCG CCCTGGGCTG TGGGCTGCCC CAGCTGCTTG CTTCCAGGAG 960
CACCATTTTC CCTTGCAAAG AAAGGACGCC ACTGTGGTTA TTGCACGTGG CTGTCGCCAG 1020
ACGTTTTCTG AAGCCAGATG AAGTGAGCCC ACTACTTTGG GGAGATCAGT CAGCTCTGTT 1080
TGTCGTCAGA ACATCTGAGC ATTCAAACAA ATGCTAGAGT TTGGGGAACG AGTATCCCCC 1140
ACTGTGAGTT 1150
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