Variant report

Variant	rs554815025
Chromosome Location	chr9:93807839-93807840
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv972278	chr9:93806856-93807852	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93801800-93809800	Weak transcription	A549	lung
2	chr9:93802400-93810800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:93806000-93809400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr9:93806200-93809400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr9:93806600-93808000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr9:93806800-93809400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr9:93807000-93808200	Enhancers	HepG2	liver
8	chr9:93807400-93808200	Enhancers	Placenta Amnion	Placenta Amnion
9	chr9:93807800-93809600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr9:93807800-93809800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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