Variant report

Variant	rs10840034
Chromosome Location	chr11:8419587-8419588
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11041904	0.82[ASN][1000 genomes]
rs11826312	0.85[AFR][1000 genomes]
rs11827424	0.90[AFR][1000 genomes]
rs11827954	0.84[AFR][1000 genomes]
rs11828529	0.83[AFR][1000 genomes]
rs58650381	0.84[AFR][1000 genomes]
rs61142266	0.82[AFR][1000 genomes]
rs7123919	0.86[AFR][1000 genomes]
rs7124356	0.83[AFR][1000 genomes]
rs73402080	0.81[AFR][1000 genomes]
rs73402082	0.82[AFR][1000 genomes]
rs7950961	0.83[AFR][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	esv1797209	chr11:8417452-8474015	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8418200-8420200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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