Variant report

Variant	rs16843812
Chromosome Location	chr2:141098362-141098363
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10460268	0.86[CHB][hapmap];0.92[CHD][hapmap]
rs10496841	0.93[CEU][hapmap];0.90[CHB][hapmap];0.92[CHD][hapmap];0.83[GIH][hapmap];0.95[JPT][hapmap];1.00[TSI][hapmap]
rs11674722	0.91[CHB][hapmap];0.87[CHD][hapmap];0.83[GIH][hapmap];0.95[JPT][hapmap];0.89[TSI][hapmap];0.82[ASN][1000 genomes]
rs11691524	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs12233220	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1474102	0.91[CHB][hapmap]
rs16843644	0.91[CHB][hapmap]
rs16843680	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs16843732	0.91[CHB][hapmap];0.92[CHD][hapmap];0.90[GIH][hapmap];0.95[JPT][hapmap];0.89[TSI][hapmap]
rs16843825	1.00[CEU][hapmap];0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16843911	0.95[CHB][hapmap];0.97[CHD][hapmap];0.90[GIH][hapmap];0.95[JPT][hapmap];0.91[MEX][hapmap];0.82[TSI][hapmap];0.89[ASN][1000 genomes]
rs16856005	0.86[CEU][hapmap];0.95[JPT][hapmap]
rs3748864	0.91[CHB][hapmap];0.95[JPT][hapmap];0.89[TSI][hapmap]
rs3748865	0.86[CHB][hapmap];0.92[CHD][hapmap];0.90[GIH][hapmap];0.95[JPT][hapmap];0.96[TSI][hapmap];0.85[ASN][1000 genomes]
rs3887578	0.91[CHB][hapmap]
rs73964214	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754266	chr2:141023643-141270786	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv875185	chr2:141055080-141179257	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	nsv1002168	chr2:141056296-141157971	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No data

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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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