Variant report

Variant	rs3018706
Chromosome Location	chr11:101490200-101490201
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10219300	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10219398	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10750613	0.81[EUR][1000 genomes]
rs10750614	0.81[EUR][1000 genomes]
rs10750615	0.81[EUR][1000 genomes]
rs10750616	0.81[EUR][1000 genomes]
rs10895138	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10895139	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10895144	0.93[EUR][1000 genomes]
rs10895148	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10895160	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11224830	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11224875	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11523959	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12280648	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12282925	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1892873	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1938830	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1938840	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1938848	0.81[EUR][1000 genomes]
rs1938852	0.81[EUR][1000 genomes]
rs1938853	0.81[EUR][1000 genomes]
rs1938854	0.81[EUR][1000 genomes]
rs1938855	0.81[EUR][1000 genomes]
rs1939449	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1939451	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1939452	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2105612	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2154992	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2154996	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2154997	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2186577	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2186578	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2186579	0.81[EUR][1000 genomes]
rs2226558	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2508244	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2508246	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2508250	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2508251	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2508252	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2508254	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2508725	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2508726	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2508727	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2508728	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2508729	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2513191	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3018703	0.80[EUR][1000 genomes]
rs3018705	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3018707	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35080821	0.83[EUR][1000 genomes]
rs41302375	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4754778	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4754780	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56134796	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6590893	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6590894	0.86[EUR][1000 genomes]
rs7107018	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7107512	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7112189	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7116889	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7119712	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7119886	0.85[EUR][1000 genomes]
rs7125321	0.89[EUR][1000 genomes]
rs7126770	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7942189	0.92[EUR][1000 genomes]
rs947992	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9988861	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 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	esv2754308	chr11:101409790-101502790	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv898331	chr11:101436689-101492630	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101487200-101490400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr11:101488200-101490400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:101489600-101490200	Enhancers	NHEK	skin

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