Tag | Content |
---|
EnhancerAtlas ID | HS111-01767 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr16:811180-812590 |
Target genes | Number: 25 | Name | Ensembl ID |
|
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr16:812078-812088 | GCCCCGCCCC | + | 6.02 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AACAACCTTT GAGCTCTTCC TGTTGTGGTG TGGATGGAAT CTGCACCTTC CATCTGGAGA 60 ACTGGGGCCG CCCCAGGCCG GGCTTCCAGC ACCAGAGCGA TGGTCAGGCT TCAGCTGGAC 120 GCAGATTTCA CCCCGCAGGG CACACGCAGA CCCATTTGTT TGGAAGCGGC AGTCCTAAGG 180 CAGTGCAGGT GCCTCCACGG CCCCAGCCCA GCTCTCCTGC AGGTGTAAAG GATGCAGATT 240 CCAGGGCCCC CCATGGCCTG CAGAGGCCCC TCAGAGCAGG AAGGGCCGGG CTCTCGGGGA 300 GCCCCCATCC CAGGTGCTGA GGTCCTTGGG TCACATGGAG CTGGGGTGGG GAGTGCCCAG 360 GTCCCCTGTG ATCCGATGGC CACGTTTCCC TCCTGGCTTC ACGCACCCCA AGGGCTGGGG 420 GTCCCACTCA CTGCCCATTT TCTGGCTGTG GGGGGGGTCT GTTTTCTTCC ACCTTCTCAA 480 GGTGTTCAGA GCCTCAGGGG CCTCCCCACT TCCTCTGGGG CCTGGGGGAG TAGAGTCTGT 540 CACCCGGAGG CTGTGTGCCT CCCCGCGACA TTCCCCAGTG GCCGGGCCGA CCAGGCAGGC 600 TCTGCCTGTG GATGGGGCTG CTGAGCATGA GCGTGTGACC CCCATTTCTG AGCTGTGGGT 660 GGACCCACCG GGCCTGGGCC AAGGTTTTCA GGAGGCAGCT CTATTCTACT CCGCCATGGT 720 GGCCTCCCTG AAAGGGGTGA GTGTAGAAGC CAGTTCCCTC TTCTGCGAGC CCCACCCCTA 780 CCCCAGGAGG ACAATTCTTG TTCAGGGAGG GTCTCCCCAC CCACTTCCCC ACCCCACAGT 840 GGCCCACAGG CCCCACCCTA GAGAGTACAA GGGGCTCCCC AGGCTGCTCA CTGGCCCAGC 900 CCCGCCCCAC CTGGACTGCA CCTGAAAATG GGCTCAGAGA GGCCAAGTGG CCCAAAAAGA 960 CGCTGCTGGG TGGGAAGGGG CGGTGGCCTC TGTGCCCGCA GTGCCCCTCC TGCCTCAAGG 1020 GTGTTGTCTG CCTGGCAGAG CCTGGGGTGT TCACAAAGCC CAGGCACCTG CAGCTGAGGG 1080 CAGGGGAGAG GGAAGGGAGC CACATCCAGG CGACGGGGCT GCTCGTCCTC CTGTGCGAGA 1140 GTGGGGAGAC TCAGGCCAGC CCAAGTGGGC GGCGGCCCCG GTTGCTTGAT CTAAGCTCTG 1200 CTCACACTGC CCTGCCCTTC TGGGAGAGGG GTGGGCGCCA ACTGACTCCT GGGCTGTCTG 1260 GGCTGGGGAC CGGGATCTCA GACCCAGCCC CTCCCCTGGA CAGGAGGAGC CAGTCCAGGG 1320 GACAGAGGGC TCAGTGGCTG GAGGGCAGGG CCAGGGTGCG GACACAAGCT GCAGGTACCA 1380 CAGAAGTTTG CTCTGGGAGC CCCTCCTGGG 1410
|