Variant report

Variant	rs2216958
Chromosome Location	chr2:205172909-205172910
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10166064	1.00[EUR][1000 genomes]
rs10176503	1.00[EUR][1000 genomes]
rs10191204	1.00[EUR][1000 genomes]
rs10202333	1.00[EUR][1000 genomes]
rs10205316	1.00[EUR][1000 genomes]
rs11891596	1.00[EUR][1000 genomes]
rs12468741	1.00[EUR][1000 genomes]
rs12472508	1.00[EUR][1000 genomes]
rs1447487	1.00[EUR][1000 genomes]
rs1447491	1.00[EUR][1000 genomes]
rs1447494	1.00[EUR][1000 genomes]
rs1470544	1.00[EUR][1000 genomes]
rs1545378	1.00[EUR][1000 genomes]
rs1550911	1.00[EUR][1000 genomes]
rs16824667	1.00[EUR][1000 genomes]
rs1992844	1.00[EUR][1000 genomes]
rs2053762	1.00[EUR][1000 genomes]
rs2121681	1.00[EUR][1000 genomes]
rs2121682	1.00[EUR][1000 genomes]
rs55700498	1.00[EUR][1000 genomes]
rs56249032	1.00[EUR][1000 genomes]
rs6709185	1.00[EUR][1000 genomes]
rs6751197	1.00[EUR][1000 genomes]
rs6751909	1.00[EUR][1000 genomes]
rs6752041	1.00[EUR][1000 genomes]
rs7575807	1.00[EUR][1000 genomes]
rs921164	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005589	chr2:205143670-205204662	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv536121	chr2:205143670-205204662	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:205171800-205173600	Enhancers	Primary neutrophils fromperipheralblood	blood

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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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