Variant report

Variant	rs60434357
Chromosome Location	chr9:93853066-93853067
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs12341726	0.97[ASN][1000 genomes]
rs12344046	0.97[ASN][1000 genomes]
rs16907148	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv1052912	chr9:93846078-93866362	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93847800-93855600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:93851600-93853200	Enhancers	HepG2	liver
3	chr9:93851800-93853200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr9:93852000-93853200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr9:93852400-93853200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr9:93852400-93853200	Enhancers	Lung	lung
7	chr9:93852600-93853600	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr9:93852600-93853800	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr9:93852600-93855400	Weak transcription	Fetal Intestine Small	intestine
10	chr9:93852600-93859800	Weak transcription	Fetal Heart	heart
11	chr9:93852600-93861600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr9:93852800-93861200	Weak transcription	NHLF	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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