Variant report

Variant	rs348670
Chromosome Location	chr12:62472436-62472437
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10877793	0.85[CEU][hapmap]
rs10877796	0.85[CEU][hapmap]
rs11174295	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11174298	0.91[CEU][hapmap]
rs11174331	0.85[CEU][hapmap]
rs12309125	0.85[CEU][hapmap]
rs1245362	0.92[CEU][hapmap];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1985820	0.85[CEU][hapmap]
rs348631	0.91[JPT][hapmap]
rs348632	0.94[JPT][hapmap]
rs348633	0.91[JPT][hapmap]
rs348640	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs348641	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs348642	0.98[ASN][1000 genomes]
rs348643	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs348644	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs348645	0.98[ASN][1000 genomes]
rs348646	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs348647	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs348648	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs348649	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs348650	0.98[ASN][1000 genomes]
rs348651	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs348653	0.98[ASN][1000 genomes]
rs348658	0.82[JPT][hapmap]
rs348665	0.91[JPT][hapmap]
rs348666	0.85[JPT][hapmap]
rs348667	0.91[JPT][hapmap]
rs348671	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs348680	0.80[CHD][hapmap];0.86[JPT][hapmap];0.81[MEX][hapmap]
rs348683	0.86[JPT][hapmap]
rs348688	0.86[JPT][hapmap]
rs348689	0.84[CHD][hapmap];0.86[JPT][hapmap];0.81[MEX][hapmap]
rs348690	0.84[CHD][hapmap];0.86[JPT][hapmap]
rs348691	0.84[CHD][hapmap];0.86[JPT][hapmap]
rs348693	0.86[JPT][hapmap]

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	nsv1039741	chr12:62046850-62491052	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv832435	chr12:62407000-62601835	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62471400-62472600	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr12:62471400-62472800	Enhancers	Fetal Heart	heart
3	chr12:62471400-62473000	Enhancers	Aorta	Aorta
4	chr12:62471800-62472600	Enhancers	Colon Smooth Muscle	Colon
5	chr12:62472000-62472800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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