Variant report

Variant	rs10121971
Chromosome Location	chr9:15546593-15546594
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 94 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs10116904	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10117524	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10118595	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10118675	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10118719	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10119257	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10119931	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10120171	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10121012	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10121911	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10123084	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10124655	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10124718	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10124746	1.00[ASN][1000 genomes]
rs10125713	0.89[EUR][1000 genomes]
rs1041529	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10962054	1.00[ASN][1000 genomes]
rs10962061	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12336383	1.00[ASN][1000 genomes]
rs12336445	1.00[ASN][1000 genomes]
rs12337310	1.00[ASN][1000 genomes]
rs12344963	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12348561	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12348564	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12348780	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12350062	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12350903	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12352398	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12353048	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs175762	1.00[ASN][1000 genomes]
rs202321	1.00[ASN][1000 genomes]
rs2064030	1.00[ASN][1000 genomes]
rs2202865	1.00[ASN][1000 genomes]
rs2665503	0.89[EUR][1000 genomes]
rs2665515	1.00[ASN][1000 genomes]
rs2737840	1.00[ASN][1000 genomes]
rs276434	1.00[ASN][1000 genomes]
rs276437	1.00[ASN][1000 genomes]
rs276438	1.00[ASN][1000 genomes]
rs276439	1.00[ASN][1000 genomes]
rs276440	1.00[ASN][1000 genomes]
rs276442	1.00[ASN][1000 genomes]
rs276445	1.00[ASN][1000 genomes]
rs276446	1.00[ASN][1000 genomes]
rs276450	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs276451	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2777951	1.00[ASN][1000 genomes]
rs2795125	1.00[ASN][1000 genomes]
rs2795128	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2821525	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2821529	1.00[ASN][1000 genomes]
rs2821542	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2821543	1.00[ASN][1000 genomes]
rs2821544	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28449490	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28497163	1.00[ASN][1000 genomes]
rs28610358	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs28735068	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28796681	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28800775	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28805077	1.00[ASN][1000 genomes]
rs28808908	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28844368	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28882210	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28893033	1.00[ASN][1000 genomes]
rs3119700	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3122701	1.00[ASN][1000 genomes]
rs3122705	1.00[ASN][1000 genomes]
rs3129711	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs365710	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs381205	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs392627	1.00[ASN][1000 genomes]
rs398117	1.00[ASN][1000 genomes]
rs398178	1.00[ASN][1000 genomes]
rs399808	1.00[ASN][1000 genomes]
rs401393	1.00[ASN][1000 genomes]
rs413356	1.00[ASN][1000 genomes]
rs415157	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs418153	1.00[ASN][1000 genomes]
rs424131	1.00[ASN][1000 genomes]
rs443563	0.84[EUR][1000 genomes]
rs592452	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7021840	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7852936	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7860339	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs796391	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs811282	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs926154	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9406518	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892625	chr9:15326251-16064850	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv892626	chr9:15389610-15694690	Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv892627	chr9:15397969-15909450	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv892629	chr9:15516375-15634326	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	esv3407839	chr9:15530438-15665653	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15544000-15551800	Weak transcription	A549	lung

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