Variant report

Variant	rs35080821
Chromosome Location	chr11:101507116-101507117
allele	AA/GG
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10750613	0.80[EUR][1000 genomes]
rs10750614	0.80[EUR][1000 genomes]
rs10750615	0.80[EUR][1000 genomes]
rs10750616	0.80[EUR][1000 genomes]
rs10895160	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1938830	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1938840	0.84[EUR][1000 genomes]
rs1938848	0.80[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	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1939451	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1939452	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2105612	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2154992	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2154996	0.84[EUR][1000 genomes]
rs2154997	0.84[EUR][1000 genomes]
rs2186577	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2186578	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2186579	0.81[EUR][1000 genomes]
rs2226558	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2508244	0.80[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs2508246	0.83[EUR][1000 genomes]
rs2508250	0.83[EUR][1000 genomes]
rs2508251	0.84[EUR][1000 genomes]
rs2508252	0.84[EUR][1000 genomes]
rs2508254	0.80[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs2508725	0.84[EUR][1000 genomes]
rs2508726	0.84[EUR][1000 genomes]
rs2508727	0.84[EUR][1000 genomes]
rs2508728	0.80[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs2508729	0.80[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs2513191	0.80[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs3018705	0.83[EUR][1000 genomes]
rs3018706	0.83[EUR][1000 genomes]
rs3018707	0.80[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs4508175	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6590893	0.89[EUR][1000 genomes]
rs6590894	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7107018	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7107512	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7112189	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7116889	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7119886	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7126770	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs947992	0.84[EUR][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	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101507000-101509600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr11:101507000-101509800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links