Variant report

Variant	rs17021215
Chromosome Location	chr3:28233562-28233563
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:28232370..28234872-chr3:28235014..28237242,2	K562	blood:

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs11129314	1.00[CHB][hapmap]
rs11916111	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11916585	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11916606	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11916686	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11918487	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11920536	0.85[AMR][1000 genomes]
rs11920615	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11923769	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11926903	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11927668	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12106806	1.00[CHB][hapmap];0.80[JPT][hapmap]
rs12107183	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12107191	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12107556	1.00[CHB][hapmap];0.80[JPT][hapmap]
rs12107565	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13069450	1.00[CHB][hapmap];0.80[JPT][hapmap]
rs13074515	1.00[CHB][hapmap]
rs17021208	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17021232	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17021238	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1873836	1.00[CEU][hapmap]
rs35178864	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4680746	1.00[CHB][hapmap]
rs55940261	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56250178	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56687471	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57267508	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57358658	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58886943	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58899029	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60163502	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60163709	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61479857	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61548543	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61633201	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6778650	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6780084	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6791708	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6793933	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6794980	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6795634	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6797580	1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6798101	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6802491	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6809163	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6809706	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6809917	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72898235	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73822327	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73822555	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73823423	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73823424	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73823425	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73823426	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73823427	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73823429	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73823432	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73823433	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73823434	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7610729	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7614914	1.00[ASN][1000 genomes]
rs7624015	1.00[CHB][hapmap];0.80[JPT][hapmap]
rs7624111	1.00[CHB][hapmap];0.80[JPT][hapmap]
rs7635045	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7638878	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7639138	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]

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	esv3328565	chr3:27991169-28915035	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv876648	chr3:28060456-28280965	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv876649	chr3:28126595-28718454	Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv998002	chr3:28208676-28252031	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:28231800-28233600	Enhancers	Muscle Satellite Cultured Cells	--

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