| Tag | Content |
|---|
EnhancerAtlas ID | HS024-16495 | Organism | Homo sapiens | Tissue/cell | Cerebellum | Coordinate | chr9:137017150-137018520 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr9:137017638-137017649 | GCAGGGTGTGG | - | 6.62 | | Klf1 | MA0493.1 | chr9:137017640-137017651 | AGGGTGTGGCC | - | 6.32 | | PLAG1 | MA0163.1 | chr9:137018068-137018082 | CACCCTTGGGCCTC | - | 6.31 | | ZNF263 | MA0528.1 | chr9:137017219-137017240 | TTCTTCACCAGCTCCTCCTCC | - | 6.21 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGTGAGTGTG GCTCTGTGTG GGGGCTGGGT CTGTGGGGAG GGCCTCCCCT GCTGGGTTCA 60
CTGCCCCTGT TCTTCACCAG CTCCTCCTCC CTCCTCTGCC CTGGGTCCGC CCCTGCAGGA 120
GGAACCTTCC TCCGTGTCCG ACCGTTCCGC CAGCTCCCCC TGACCGCCCG CTGGCTCTGT 180
TGCTCCTTCT GGTGCAGTTT TCCTGCCATG GCCTTTCTCT TGGGCCAGCC TGGGGCTCCT 240
CCACCTGTGC TGTCGGCCTC ACTCCGGCTG CTCACTGGAG TCCTCTGGGC AGCCCCATTG 300
CCTCCTGGCT TCGGGCCCCT GCTGTCGTGC CAGCCTCTTG GATCATTCCT TGAGTGACCG 360
GCTGAGTGCC TGCCCATCTG CTGGGGGTGC TGCCGAGGTG GATGGAGGTG TCCTGGGGGC 420
ACGGAGGACA GGCCTGAGGA GAGGAAGGAG GGACGTGGCG TGGCCTGGAT GGGAAGGCCA 480
GGTGCTGGGC AGGGTGTGGC CTGAGGGTCT GTGACGGCCC GGGGTTCCCA GCTGCCCCTT 540
GCAGAGCCTG CAGAAAGGAG CGGAAGGGTT TTCATCCGGG GAGTGTTCGT GTTTAAGAAG 600
CCTAGGCTAG ATGTGTGGGA TGGGGCGCAC CTTGAGGAGG GAGCTGGGTG GTGAGGATGG 660
GGGGATGGAC CCCCGTGTGG GGAGGCACCC CGTTTGCGCC CTTCTTCCCT CTAGTCTGTC 720
ATAGCCTGCT GGCCTAGCTG AGACCAAGCC CCACAGGCTG GGAGGCTATC TGTGGCAGGA 780
ATGTGTCTCC CCGCAGTCCA GGAGGCTGTG GTCAGGATTG AGGAGGCCTC TTCTTGGCTT 840
ATAGACGCTG CCTTACCCTG GCTTCACACC AGTGTCCCTG GTGCCTCCGT GTGTCCAAAT 900
GTCCTCTTGT AAGGACACCA CCCTTGGGCC TCATTTTCAC TCTGTCGCCC TCTTTGAAGG 960
CCCTGTCTCC AGTACACTCG CCTCTGAGGC TCTGGAGGCT TGGGCTTCAG CATGAGTCCC 1020
CTTGCCACAG CGGTCTTTAT AGCTTCCTGC CTTGTGGGGC CAGCCTTTTG CCATGCATCT 1080
CTCCTGATTG AGATCACACC GCACTTGGTG TCCCCTGGAC GGGCCACCTG TGCTCAGTTG 1140
TGTGCGCCGC TGTTGTGTGA GCACACGTAA CCCTCACGGC CACCTCTGAG GAGGGGGGTT 1200
GTCCTCATCC TGCATAGAGG CTCATTCACT AGCCCAAAGC TCCACAGCAA GCAGGTGCAG 1260
GGACTGGGAT TCCAGCCTGG GCGCCCCTGA GCCCAGGGTG GGGACGGAGG GGTCGCTGCA 1320
TAGCAGTTTT CCCATCGGCG TCTCCTCAGG TCTAGCGAGT TAGACCCTTC 1370
|
| |
|
|
|
