Tag | Content |
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EnhancerAtlas ID | HS184-11938 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr16:1417350-1417650 |
Target genes | Number: 15 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr16:1417484-1417502 | CCCTCCCTCCCTCCCTCC | - | 6.03 | EWSR1-FLI1 | MA0149.1 | chr16:1417488-1417506 | CCCTCCCTCCCTCCCTCC | - | 6.03 | EWSR1-FLI1 | MA0149.1 | chr16:1417492-1417510 | CCCTCCCTCCCTCCCTCC | - | 6.03 | EWSR1-FLI1 | MA0149.1 | chr16:1417496-1417514 | CCCTCCCTCCCTCCCTCC | - | 6.03 | ZNF263 | MA0528.1 | chr16:1417484-1417505 | CCCTCCCTCCCTCCCTCCCTC | - | 7.97 | ZNF263 | MA0528.1 | chr16:1417488-1417509 | CCCTCCCTCCCTCCCTCCCTC | - | 7.97 | ZNF263 | MA0528.1 | chr16:1417492-1417513 | CCCTCCCTCCCTCCCTCCCTC | - | 7.97 | ZNF263 | MA0528.1 | chr16:1417496-1417517 | CCCTCCCTCCCTCCCTCCCCC | - | 8.55 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | CTGAAACCCA GGGCCCGTCT CAGCACCCCC CACCTCACCT GTGCCACCTG CAGACCCTCT 60 TGCCTGTGTC ACCAGCGATC CTCCCCTCCC CTCCCCAGCA TCAGCTGTGG CCCCCTCACC 120 TGAGACCCCT GCGGCCCTCC CTCCCTCCCT CCCTCCCTCC CTCCCCCTCC CGTCTCACCC 180 CCCACACGCT CACCTGAGTC ACCTGCGGCC CTCCCTCCCT CCCCTCCCAT CTCACCCCCA 240 CACGCTCACC TGAGTCCCCT GCGGCCCTCC CTCCCCCTCA CCTGTCTGGC CCCCCCACAC 300
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