| Tag | Content |
|---|
EnhancerAtlas ID | HS047-27834 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr5:153902860-153904050 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr5:153903757-153903770 | TTCTGGAATATTC | + | 6.48 |
| | | 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 |
| GH05I154522 | chr5 | 153902321 | 153905099 |
| Enhancer Sequence | AAGCACATGG CGCCTGGCAC ATTGGTCACC CTCAATCCAT GGCATTGGAT CTTTGTCACC 60
TGACTGTCAT CATCCCTTCT GACTCTCAGT CCCTCCTCTG AACAACAGCT GTGTGTTGGC 120
CCCATTCATG TCCCACCAAT GCCCAGTCCT TTAGGGGGCT CCCCAGCTAG CCAAGGTGAC 180
CCCATGCTAA CATTTCCCAA GCTCTTTCCT CAAATTTTAT CTCCATCATC AATGACCAAC 240
TCCTCTGTGT CAGAGGCAAA CAGCTCCCAC CCGTATTTAT TTCACCCCAG CTTTGTCTAT 300
TTATAGGAAG CTGGCTTGTC CTGACGCTGT TTCTGTTAAC AAGGCAGGCA TCTCAGCCAA 360
CTGGGCAGAA AAGCAGCAGA AACCTTCAGT CCTGCCCATA AAGGCCCCAG AAATGTCTCT 420
GCCTCCAGAG GTTTTTGAGA AACTGCTGCA AGGGGAATTA TGAGTGTAAA CTTGCCCCCT 480
CCCTCTGCCC GCCCCCCAGC CCTCTCATCT GGACAATAAC AGCTCCCATC TCATCTCTGA 540
GAAACCATTC CCGAAGGTTC CAGCTGAGTG CAGGATTAGG CCTCAGGGTG GCAATTAGCT 600
GATAAGGCGA TGACTTCACC CAGAGCAGAG AGAGCCTGGC TAGCTGGAGC CTGTCCCTGC 660
AGGACACCCT GCCCTGGGCC TCTCTCCCTG GACTTAGAGA CAGGAACCCT GGCCCAAGGC 720
TTGGGGAAGT CTCTTCCCCT CTCTGGACCT CTGATTGCCC CTGTGTGAAA TGGAGCATGT 780
TCTGACCTTC ACAGGCTTGT GGGAAGCTCC AGTAAAATAA GAAATAAGAT CTTGCTCAGA 840
AAGAATCCCT GGCAGCAGTG CATTGCTGAC CATAGACAAC CATAGAACTG GAGCCTTTTC 900
TGGAATATTC CTGAAGGAAC AAAGAAAAGA GGCACTGGCC AGGGAATCAG GTGGACCTGA 960
GTTTCTGAGC ACAGGCCCTG TGTTCACCAG CTGTGTGCTC TCAAGCAGGC TGCCTCCCTT 1020
TCCTCTCTGT AAAATGGGAC AGTGTTTGTG CCTTGTCTTC CTCGCACATG GTTTTGAGAT 1080
GCAGAGATAA CTGAGGAAGG AGAGCTGAGC GGATAAGATC ACAGGTTTCA GAGCATGTGG 1140
GCCTGGCTTC GAGTGCCTGT TTGACCCCTT ACTAACTGTG TGCCTTTATG 1190
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