Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10166403	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10167244	0.86[JPT][hapmap];0.80[EUR][1000 genomes]
rs10188926	0.86[JPT][hapmap]
rs10194540	0.86[JPT][hapmap]
rs10201067	0.86[CEU][hapmap];0.84[EUR][1000 genomes]
rs10202760	0.86[JPT][hapmap]
rs11894208	0.88[JPT][hapmap]
rs1283310	0.82[CEU][hapmap]
rs13383863	0.85[JPT][hapmap]
rs13388956	0.86[JPT][hapmap]
rs13393577	0.86[JPT][hapmap]
rs13400881	0.86[JPT][hapmap]
rs13413335	0.85[JPT][hapmap]
rs13417523	0.82[JPT][hapmap]
rs1394780	0.86[JPT][hapmap]
rs4106226	0.86[CEU][hapmap];0.86[EUR][1000 genomes]
rs6435701	0.82[CEU][hapmap]
rs6712295	0.86[JPT][hapmap]
rs6756468	0.86[JPT][hapmap]
rs7565257	0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834527	chr2:213115966-213334308	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1014680	chr2:213142147-213301614	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1004573	chr2:213186537-213365252	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
4	nsv875811	chr2:213200920-213347104	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Symmetrical dimethylarginine levels	24159190	GWAS catalog

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213294600-213298600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr2:213296800-213298800	Weak transcription	Fetal Heart	heart

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