Variant report

Variant	rs12491904
Chromosome Location	chr3:157046870-157046871
allele	A/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]
rs11718332	0.83[CEU][hapmap];0.80[EUR][1000 genomes]
rs12489754	0.88[CEU][hapmap]
rs12491052	0.83[CEU][hapmap];0.80[EUR][1000 genomes]
rs12491934	0.82[CEU][hapmap];0.80[EUR][1000 genomes]
rs1500913	0.88[CEU][hapmap];0.80[EUR][1000 genomes]
rs1500914	0.88[CEU][hapmap];0.80[EUR][1000 genomes]
rs1566520	0.88[CEU][hapmap]
rs55735313	0.80[EUR][1000 genomes]
rs56210074	0.80[EUR][1000 genomes]
rs56333827	0.80[EUR][1000 genomes]
rs60979231	0.80[EUR][1000 genomes]
rs924515	0.88[CEU][hapmap];0.80[EUR][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	esv275099	chr3:157046192-157049852	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:157015600-157048400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:157030600-157047000	Weak transcription	Osteobl	bone
3	chr3:157036000-157047800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr3:157036800-157053000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr3:157039800-157051000	Weak transcription	HUVEC	blood vessel
6	chr3:157041000-157065600	Weak transcription	Pancreas	Pancrea
7	chr3:157046200-157047000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr3:157046400-157047000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr3:157046400-157047000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr3:157046400-157047600	Enhancers	NHDF-Ad	bronchial
11	chr3:157046600-157048000	Enhancers	NHLF	lung
12	chr3:157046600-157049400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:157046800-157047200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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