Variant report

Variant	rs2841683
Chromosome Location	chr9:96159366-96159367
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10117236	0.80[ASN][1000 genomes]
rs10117697	0.81[ASN][1000 genomes]
rs10217595	0.80[ASN][1000 genomes]
rs10992720	0.86[CHB][hapmap];0.92[JPT][hapmap];0.94[ASN][1000 genomes]
rs12555823	0.90[ASN][1000 genomes]
rs2266010	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4255201	0.88[CHB][hapmap];0.93[JPT][hapmap];0.91[ASN][1000 genomes]
rs55846141	0.80[ASN][1000 genomes]
rs55893789	0.85[ASN][1000 genomes]
rs7863760	0.80[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96153400-96161000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:96156000-96160400	Weak transcription	Lung	lung
3	chr9:96156200-96160200	Weak transcription	Placenta	Placenta
4	chr9:96159000-96160600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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

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