Variant report

Variant	rs1511211
Chromosome Location	chr2:167784900-167784901
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11884668	1.00[CEU][hapmap];0.91[CHB][hapmap];0.82[LWK][hapmap];0.85[YRI][hapmap]
rs1397700	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[YRI][hapmap]
rs1397701	0.82[CHB][hapmap]
rs1511200	1.00[CHB][hapmap];0.95[JPT][hapmap];0.82[LWK][hapmap]
rs1511210	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[YRI][hapmap]
rs1567534	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.83[YRI][hapmap]
rs7564737	1.00[CEU][hapmap];0.86[CHB][hapmap];0.82[LWK][hapmap];0.92[YRI][hapmap]

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	nsv529384	chr2:167143465-167958752	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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