| Tag | Content |
|---|
EnhancerAtlas ID | HS037-41214 | Organism | Homo sapiens | Tissue/cell | ESC | Coordinate | chr9:137040250-137041150 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr9:137040555-137040573 | CCCAGCTTCCTCCCTTCC | - | 6.36 | | KLF16 | MA0741.1 | chr9:137040472-137040483 | GGGGGCGGGGC | - | 6.02 | | KLF16 | MA0741.1 | chr9:137040489-137040500 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr9:137040473-137040483 | GGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr9:137040490-137040500 | GGGGCGGGGC | - | 6.02 | | ZNF263 | MA0528.1 | chr9:137040520-137040541 | GGAGGAGGAAGGTGATGGGGT | + | 6.93 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 137040428 | 137040559 | | chr9 | 137040251 | 137041027 |
| Enhancer Sequence | AACCAGCTCT AAGCAGATGA TTTCTGGATT TGAGCCATTC AGGTTCTGGG AGCTGGGGAA 60
ACTCATTTAG GGGTGGGCAG AGCTCGTTCC TGAGGAAACA GCGTGGAGGA CGAGTTGGAG 120
TTTGCCAGGG AAGAGGGGAA GGAGAGGGCT CTGGTAAGAA GAGACAGCTC TGCAAAGGCC 180
CTGAGGCTGG GAAGAGCAGC CGCTCCCCAA GGACAGCTAG GCGGGGGCGG GGCCCAGGCG 240
GGGGCGGGGC CCAGGCGGGG GCGGAGCCAG GGAGGAGGAA GGTGATGGGG TCAGATTCCA 300
CAGGACCCAG CTTCCTCCCT TCCCTGAGAG GTGGTTTGGG CAGAGGTGGG CAGCATGGAG 360
GCGGTGGCCC AGGGAGTCCC TGTGGTTGCC CGGGTGGAGT GCGGGGCTGG CCTGCCCCGG 420
TGGGGACATA CGCGCTCCAG GCACCCAGCA GCCCTCACCC AGCCCATCCG TCTTGCCCCG 480
GGCCCCCGGG TGCTGCCGTC TGGAGGGTGC TCTGTCTGGG CCTTGCCCTG GGGAGGTGGC 540
CAGCCCAGAT CCTCTACAAA CAGCTCGCCC CTCCCAGCTG CCCCCATCCC CTGATGGCCC 600
CCACTGTGGG AGATGCTGCT TTGGAGAGGG GCAGGAAGTG TCGCTGTGTT GGAAATCTGG 660
GGGCGTGGGT CTGGAGGTGC ACGCTCGATG CCCCTGCCCA CACGGGGTCT GTCACGGTGC 720
CGGGTTCTGA GGGGCTGGGG GGGCCCAGGG TGGGCTGAAG GACCCAGCGC AGTGGGTGAC 780
AGAGCAGGAG GTGCTCCCAG AGCTGTCCTT GGTGAGGGAG GTGTGGCGGT CACTGGTGGG 840
GGCTTCTGTT GGTCCCTCCT GCTGTGAGGG GCGCTGCGTC CACTTGGGGG CAGCTCTGTC 900
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