Variant report

Variant	rs10895193
Chromosome Location	chr11:101631933-101631934
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:101631523..101632519-chr11:101671488..101672112,2	MCF-7	breast:

Extended variants
information (count: 75 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1006330	0.91[ASN][1000 genomes]
rs10459002	0.89[ASN][1000 genomes]
rs10750618	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10791521	0.83[AMR][1000 genomes]
rs10895191	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10895203	0.80[ASN][1000 genomes]
rs10895204	0.80[ASN][1000 genomes]
rs11224994	0.91[ASN][1000 genomes]
rs11224995	0.87[ASN][1000 genomes]
rs11225004	0.83[ASN][1000 genomes]
rs11225005	0.83[ASN][1000 genomes]
rs11225011	0.82[ASN][1000 genomes]
rs11225012	0.82[ASN][1000 genomes]
rs11225015	0.81[ASN][1000 genomes]
rs11225018	0.80[ASN][1000 genomes]
rs12223480	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12361399	0.92[ASN][1000 genomes]
rs12361929	0.92[ASN][1000 genomes]
rs12365011	0.80[ASN][1000 genomes]
rs17746310	0.92[ASN][1000 genomes]
rs1939034	0.80[ASN][1000 genomes]
rs1939035	0.80[ASN][1000 genomes]
rs1939043	0.91[ASN][1000 genomes]
rs1939046	0.92[ASN][1000 genomes]
rs1939053	0.83[ASN][1000 genomes]
rs1939055	0.81[ASN][1000 genomes]
rs1939064	0.91[ASN][1000 genomes]
rs1939071	0.82[AMR][1000 genomes]
rs1939072	0.92[ASN][1000 genomes]
rs1939073	0.83[AMR][1000 genomes]
rs1939437	0.82[AMR][1000 genomes]
rs1939458	1.00[CHB][hapmap];0.90[CHD][hapmap];0.93[JPT][hapmap]
rs1939460	0.92[ASN][1000 genomes]
rs1954765	0.88[ASN][1000 genomes]
rs2105613	0.91[ASN][1000 genomes]
rs2155057	0.81[AMR][1000 genomes]
rs2155058	0.81[AMR][1000 genomes]
rs2155060	0.91[ASN][1000 genomes]
rs2155061	0.82[AMR][1000 genomes]
rs2155062	0.91[ASN][1000 genomes]
rs2155063	0.82[ASN][1000 genomes]
rs2186609	0.91[ASN][1000 genomes]
rs2186610	0.82[AMR][1000 genomes]
rs4414186	0.81[ASN][1000 genomes]
rs4429028	0.83[ASN][1000 genomes]
rs4503501	0.80[ASN][1000 genomes]
rs4548585	0.81[ASN][1000 genomes]
rs4586114	0.86[ASN][1000 genomes]
rs4754790	0.90[ASN][1000 genomes]
rs4754791	0.92[ASN][1000 genomes]
rs4754792	0.90[ASN][1000 genomes]
rs4754798	0.89[ASN][1000 genomes]
rs4754801	0.82[ASN][1000 genomes]
rs4754803	0.81[ASN][1000 genomes]
rs4754804	0.81[ASN][1000 genomes]
rs4754808	0.80[ASN][1000 genomes]
rs4754809	0.80[ASN][1000 genomes]
rs55854918	0.82[ASN][1000 genomes]
rs56245539	0.91[ASN][1000 genomes]
rs61916463	0.90[ASN][1000 genomes]
rs6590918	0.81[AMR][1000 genomes]
rs7105933	0.91[ASN][1000 genomes]
rs72986459	0.85[ASN][1000 genomes]
rs732086	0.82[AMR][1000 genomes]
rs7929894	0.91[ASN][1000 genomes]
rs7931237	0.88[ASN][1000 genomes]
rs7949648	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898330	chr11:101243644-101722031	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1052159	chr11:101439655-101853293	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1051457	chr11:101446705-101837650	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv530645	chr11:101451416-101778666	Bivalent/Poised TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv898332	chr11:101562004-101732566	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv832249	chr11:101571819-101749073	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv832250	chr11:101617934-101804020	Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv430425	chr11:101626575-101741691	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101631200-101632000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr11:101631400-101632800	Enhancers	Hela-S3	cervix
3	chr11:101631800-101632200	Enhancers	A549	lung

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