Variant report

Variant	rs11639005
Chromosome Location	chr15:54847677-54847678
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10152437	0.96[CEU][hapmap];0.91[EUR][1000 genomes]
rs10152571	0.82[ASN][1000 genomes]
rs10468008	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10468009	0.84[EUR][1000 genomes]
rs11071072	0.82[CEU][hapmap]
rs11071087	1.00[CEU][hapmap];0.91[CHB][hapmap];0.89[CHD][hapmap];0.95[JPT][hapmap];1.00[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap];0.81[ASN][1000 genomes]
rs11071088	0.82[ASN][1000 genomes]
rs11636573	0.80[CEU][hapmap]
rs11639014	1.00[CEU][hapmap];0.91[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];1.00[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs12437724	0.91[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs12443186	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs12900512	0.90[ASN][1000 genomes]
rs12908706	0.81[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12909682	0.91[CHB][hapmap];0.90[JPT][hapmap];0.83[ASN][1000 genomes]
rs12914472	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs12916626	1.00[CEU][hapmap];0.86[CHB][hapmap];0.84[CHD][hapmap];0.90[JPT][hapmap];1.00[MKK][hapmap];0.88[TSI][hapmap];1.00[YRI][hapmap]
rs1356859	0.88[CEU][hapmap]
rs16974753	0.88[CEU][hapmap];0.91[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap]
rs1818705	0.95[CHB][hapmap];0.86[CHD][hapmap];0.85[GIH][hapmap];0.90[JPT][hapmap];0.91[MEX][hapmap];0.92[ASN][1000 genomes]
rs1851001	0.83[ASN][1000 genomes]
rs1851007	0.91[ASN][1000 genomes]
rs1851008	0.85[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs1973747	0.91[ASN][1000 genomes]
rs2056342	0.95[CHB][hapmap];0.90[JPT][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2456976	0.89[CEU][hapmap]
rs2553218	0.84[MEX][hapmap]
rs2553222	0.80[JPT][hapmap]
rs2553223	0.80[JPT][hapmap]
rs2681969	0.87[ASN][1000 genomes]
rs2899546	0.89[CEU][hapmap]
rs34301708	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4109295	0.89[CEU][hapmap]
rs495769	0.88[ASW][hapmap];0.89[CEU][hapmap]
rs533450	0.85[CEU][hapmap]
rs540090	0.89[CEU][hapmap]
rs546169	0.89[CEU][hapmap]
rs589611	0.88[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap];0.88[LWK][hapmap];0.96[MKK][hapmap];0.84[TSI][hapmap];1.00[YRI][hapmap]
rs605869	0.89[CEU][hapmap];0.89[GIH][hapmap];0.88[TSI][hapmap]
rs640442	0.85[CEU][hapmap]
rs6493687	0.89[CEU][hapmap];0.91[GIH][hapmap];0.88[TSI][hapmap]
rs6493690	0.91[ASN][1000 genomes]
rs7163424	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs8023595	0.91[CHB][hapmap];0.80[GIH][hapmap];0.90[JPT][hapmap];0.96[MEX][hapmap];0.88[ASN][1000 genomes]
rs8023918	0.95[CHB][hapmap];0.90[JPT][hapmap];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8025195	0.85[CEU][hapmap]
rs8026697	0.82[AFR][1000 genomes]
rs8032415	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8039515	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs8040060	0.80[JPT][hapmap]
rs8040774	0.80[JPT][hapmap];0.87[MEX][hapmap]
rs8041282	0.86[CHB][hapmap];0.85[JPT][hapmap];0.82[ASN][1000 genomes]
rs8042341	0.91[CHB][hapmap];0.85[JPT][hapmap];0.83[ASN][1000 genomes]
rs885204	0.80[CEU][hapmap]
rs9302181	1.00[CEU][hapmap];0.86[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];1.00[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap]

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	nsv817539	chr15:54132584-55095235	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1038660	chr15:54756184-55039913	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
3	nsv904236	chr15:54820897-54912439	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:54811000-54869600	Weak transcription	Aorta	Aorta
2	chr15:54839800-54858800	Weak transcription	Fetal Lung	lung

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