| Tag | Content |
|---|
EnhancerAtlas ID | HS064-00049 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr1:6488480-6489330 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:6489155-6489173 | GGAGGGAGGGAGGGAGGG | + | 6.03 | | EWSR1-FLI1 | MA0149.1 | chr1:6489159-6489177 | GGAGGGAGGGAGGGAGGG | + | 6.03 | | ZNF263 | MA0528.1 | chr1:6489152-6489173 | TGGGGAGGGAGGGAGGGAGGG | + | 7.27 | | ZNF263 | MA0528.1 | chr1:6489156-6489177 | GAGGGAGGGAGGGAGGGAGGG | + | 7.97 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 6488945 | 6488995 | | chr1 | 6489207 | 6489325 | | chr1 | 6488576 | 6488676 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I006426 | chr1 | 6486087 | 6488616 |
|
Enhancer Sequence | TAAGATCACC CCTCTTAAGG GGTCCTCTGG GTGGGCTGGG CCAGGGCTTT GGGGGATGCC 60
TGGGATTTTC CACGCCTCTC TGGCACTCCA GGGCAATGAT CCCTCCAGTG GCCATCCTGG 120
GGCCAGAGGG CCAGGCCAGA GAAATGGCTC CCACTCAACA TGAAATTTTC CCCTCCTGGA 180
AAACCCCTTC TGGGGCTGCC CCCAGAGCCC TGCAAGCAGG TGCTCCCAGC ATCCTCAGCT 240
GCCCGGCCGC ACACAGCTGG ACCTGGGAGG CTGGGCACAC AGGCCAAGGT CACCTGTTCC 300
CCTTGGGCTG CTTCTGCCGC AGGGGCTCTC TCTGGCTCAG GCTGTGCTCA TTTGCAAGAC 360
TGTTCAGGAT GGAGTCGGGG GCAGCAAGGG CAGGAGCGCC TCCTAGGCCC TAGTCAAACA 420
GGCAGAAAGG GAACCCCATC AGTTACCAAG CAGTTAAGGG AGAAAGGCCC CTCCCAGACC 480
CCCACCCCAC CTCCTGGCCC CAGAGCCCCT GGCTGGAGGC CATCCAGAGA GCATCTTGTT 540
ATCTCCTGTG GCCCCTCAGC CCGTTCCTAC TATCAAGGGA AGCATGGGGA TCCCAAACCT 600
CCTGGGGAGT GGGCTGGGAG CTCCCCTGGG TGGGGTGGGG GGTCACACAG AGCAGGGGGC 660
ATGTGTGAGT CTTGGGGAGG GAGGGAGGGA GGGAGGGACT CAGGTGTTAG GTGCGCCTGG 720
GGAGGCAGGG ATCCTGGGGA AAGCTGCCCA GGGCCTGTCT GAGAGGGTAG GGTGCCAGAT 780
GCCACAGGGG TCTGAGCGGG GAGTGGGGTG CTCTGATGGG TGACCCTCAT TAGTCTAAGT 840
GGGAGCCTGA 850
|
