Tag | Content |
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EnhancerAtlas ID | HS108-32652 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr5:132443700-132444640 |
SNPs | Number: 3 | 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 | chr5:132443850-132443862 | GATTGTTTATTT | + | 6.62 |
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| 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 |
GH05I133108 | chr5 | 132444093 | 132444293 |
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Enhancer Sequence | CACCATGCCT GGCCTACATT TTTACACACA CAATGTAGGT TATAAAACTA CATAGCCTCT 60 CATGTTTTGA AAGAACATTA AATGGGTTTG CAATAAAAAA GCCAGAAGGA TTTTCCCAGA 120 TGAAGTGGTT TTTAGGGTGG GATTGTGGGT GATTGTTTAT TTTTGCTTGT TTCTGTTTTC 180 AGAGTTTGCT ACAATAAGCA TTTAGGGCCA GGCATGGTGG CTCATGCCTG TAATCCCAGC 240 CAAAGTGGGA GGATCTCTTG GGTCCAGGAG TTCAAGACCA GCCTGGGCAA CATGGGGAGA 300 CAAGCCCCTA CCCCCCACCG CCTCCTGTCA CTAATAAAAG CATTTAGGAA TTTTATAATG 360 TTAAGAAAAC TAGAAGTGTG TTTTAAGAAG AATGGCTCCA AGGTTTCAAA CCTAGAATAC 420 GGGATATGAT TGTACATGTG GAGCTTCTAG TCTTGAGTCA TTGGAGATGT GGTGGGAGTT 480 TAGATTGAGA AGTTTTCCTG GGTGGGGTTG AGACATCGAA GCTCCAGGTG GGTGTGGATG 540 GAAGCTTTTG GGGCTGGAGT CGTGTTCCTC ATTGACGGGA TGAAGGCTTG TGTTGAGATG 600 TGTTAGGAAG AGGAAGTAAA AGCTTTGAAA GAAGGAACTG CCAGAGAGGA GTTATGATGC 660 ATAAAGCATG TTGGGAGGAA GGGAGCTAGA GATGTGAGAT GTGGCAGTGG CCAGCAGGGT 720 TAGATGCTTC AGTAGGGTGG GAGCTGGGTG GGGTGAAGGG GCTTGAGGTG AGGCTGCAGG 780 TGCTGAGTAC TTGGTCAAGA AGCTTGGCCT CAGCCGCCCC GTCCGGGAGG GAGGTGGGGG 840 GGTCGGCCCC CCGCCCGGCC AGCCGCCCCG TCCGGGAGGG AGGTGGGGGG GGTCAGCCCC 900 CCCGCCCAGC CAGCTGCCCT GTCCGGGAGG TGAGGGGCGC 940
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