Variant report

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

rs_ID	r²[population]
rs11068425	0.90[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs2271984	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2291909	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2293053	0.96[ASN][1000 genomes]
rs3782195	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AFR][1000 genomes]
rs41432944	0.80[ASN][1000 genomes]
rs58807700	0.96[ASN][1000 genomes]
rs73401890	0.96[ASN][1000 genomes]
rs73401892	0.96[ASN][1000 genomes]
rs7960451	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs9658449	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs9658450	0.85[ASN][1000 genomes]
rs9658462	0.96[ASN][1000 genomes]
rs9658463	1.00[CHB][hapmap];0.96[ASN][1000 genomes]
rs9658496	0.80[ASN][1000 genomes]
rs9658501	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs9658508	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs9658512	0.80[ASN][1000 genomes]
rs9658515	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs9658565	1.00[YRI][hapmap];0.80[AFR][1000 genomes]

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	nsv832526	chr12:117530234-117723821	Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv510592	chr12:117618872-117684713	Bivalent/Poised TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117651800-117696000	Weak transcription	Brain Anterior Caudate	brain
2	chr12:117660000-117727400	Weak transcription	Psoas Muscle	Psoas
3	chr12:117666200-117704200	Weak transcription	Brain Angular Gyrus	brain
4	chr12:117670000-117687800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr12:117674800-117706600	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr12:117678800-117687600	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr12:117681400-117687000	Weak transcription	NHEK	skin
8	chr12:117681400-117687600	Weak transcription	Skeletal Muscle Male	skeletal muscle

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