Variant report

Variant	rs11211897
Chromosome Location	chr11:106627976-106627977
allele	A/C
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]
rs10890577	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11211884	0.95[ASN][1000 genomes]
rs11823116	0.94[ASN][1000 genomes]
rs1487903	0.95[ASN][1000 genomes]
rs1938622	0.95[ASN][1000 genomes]
rs2200658	0.94[ASN][1000 genomes]
rs2220376	0.96[ASN][1000 genomes]
rs3907374	0.97[ASN][1000 genomes]
rs4121676	0.96[ASN][1000 genomes]
rs6588919	0.90[ASN][1000 genomes]
rs6588921	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7128815	0.97[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	nsv898359	chr11:106523574-106656863	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106552800-106628200	Weak transcription	Pancreas	Pancrea
2	chr11:106607800-106629000	Weak transcription	Fetal Lung	lung
3	chr11:106627000-106656800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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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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