Variant report

Variant	rs11917335
Chromosome Location	chr3:86820923-86820924
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 101 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs10470570	0.86[EUR][1000 genomes]
rs11127959	0.88[EUR][1000 genomes]
rs11714652	0.81[EUR][1000 genomes]
rs11718876	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11718877	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11718975	0.86[EUR][1000 genomes]
rs11919691	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12487818	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12489293	0.81[EUR][1000 genomes]
rs12489298	0.81[EUR][1000 genomes]
rs12489313	0.81[EUR][1000 genomes]
rs12493521	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12495229	0.83[EUR][1000 genomes]
rs12495954	0.85[EUR][1000 genomes]
rs12637947	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1370209	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1370210	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1370212	0.87[EUR][1000 genomes]
rs1437048	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1437049	0.85[EUR][1000 genomes]
rs1437055	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1583577	0.84[EUR][1000 genomes]
rs1583578	0.81[EUR][1000 genomes]
rs17364877	0.87[EUR][1000 genomes]
rs1808799	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2043685	0.83[EUR][1000 genomes]
rs2083018	0.88[EUR][1000 genomes]
rs2118188	0.81[EUR][1000 genomes]
rs2118189	0.81[EUR][1000 genomes]
rs2118190	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2118191	0.82[EUR][1000 genomes]
rs2118192	0.82[EUR][1000 genomes]
rs2164647	0.81[EUR][1000 genomes]
rs2324795	0.81[EUR][1000 genomes]
rs28453822	0.88[EUR][1000 genomes]
rs28553515	0.81[EUR][1000 genomes]
rs28894812	0.82[EUR][1000 genomes]
rs35309716	0.87[EUR][1000 genomes]
rs36015800	0.81[EUR][1000 genomes]
rs4425259	0.81[EUR][1000 genomes]
rs4572769	0.82[EUR][1000 genomes]
rs4855148	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4855174	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55711545	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55719700	0.86[EUR][1000 genomes]
rs56044242	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs57877392	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs59662471	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6775872	0.86[EUR][1000 genomes]
rs6777551	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6779214	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6782806	0.81[EUR][1000 genomes]
rs6807530	0.81[EUR][1000 genomes]
rs728179	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs728180	0.85[EUR][1000 genomes]
rs73133829	0.85[EUR][1000 genomes]
rs73137958	0.81[EUR][1000 genomes]
rs73137985	0.81[EUR][1000 genomes]
rs73139911	0.81[EUR][1000 genomes]
rs73139914	0.81[EUR][1000 genomes]
rs73139922	0.81[EUR][1000 genomes]
rs73139923	0.81[EUR][1000 genomes]
rs7630849	0.82[EUR][1000 genomes]
rs7631441	0.87[EUR][1000 genomes]
rs893165	0.84[EUR][1000 genomes]
rs920188	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9631517	0.81[EUR][1000 genomes]
rs9756254	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9815344	0.88[EUR][1000 genomes]
rs9815450	0.91[EUR][1000 genomes]
rs9816006	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9818400	0.85[EUR][1000 genomes]
rs9819570	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9819897	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9821486	0.90[EUR][1000 genomes]
rs9833108	0.90[EUR][1000 genomes]
rs9841059	0.90[EUR][1000 genomes]
rs9844776	0.82[EUR][1000 genomes]
rs9850281	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9858679	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9859483	0.84[EUR][1000 genomes]
rs9862624	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9864625	0.81[EUR][1000 genomes]
rs9866183	0.89[EUR][1000 genomes]
rs9881535	0.82[EUR][1000 genomes]
rs9985323	0.84[EUR][1000 genomes]
rs9985324	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877116	chr3:86518318-86964922	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv1829775	chr3:86534927-86822085	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv877117	chr3:86665408-86927574	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	esv1794028	chr3:86684769-86822085	Enhancers Active TSS Weak transcription ZNF genes & repeats	lncRNA	11 gene(s)	inside rSNPs	n/a
5	esv1827728	chr3:86684769-86822085	Enhancers Weak transcription ZNF genes & repeats Active TSS	lncRNA	11 gene(s)	inside rSNPs	n/a
6	nsv877118	chr3:86722823-86927574	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv877119	chr3:86722823-86952516	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv877120	chr3:86722823-86961118	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv877121	chr3:86732817-86916882	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv877122	chr3:86732817-86927574	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	nsv877123	chr3:86732817-86952516	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
12	nsv877125	chr3:86794501-86916882	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
13	nsv877126	chr3:86794501-86927574	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
14	nsv3902	chr3:86808374-86821132	Enhancers Active TSS	lncRNA	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:86820800-86821200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:86820800-86821400	Active TSS	Spleen	Spleen

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