Variant report

Variant	rs11241172
Chromosome Location	chr5:111893246-111893247
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	chr5:111887607..111889700-chr5:111892241..111894417,2	K562	blood:

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10038874	0.86[EUR][1000 genomes]
rs10050436	0.87[EUR][1000 genomes]
rs10055787	0.87[EUR][1000 genomes]
rs10055908	0.86[EUR][1000 genomes]
rs10056032	0.87[EUR][1000 genomes]
rs10060366	0.85[EUR][1000 genomes]
rs10060474	0.87[EUR][1000 genomes]
rs10062535	0.85[EUR][1000 genomes]
rs10062917	0.87[EUR][1000 genomes]
rs10063938	0.87[EUR][1000 genomes]
rs10064939	0.87[EUR][1000 genomes]
rs10065523	0.87[EUR][1000 genomes]
rs10065629	0.87[EUR][1000 genomes]
rs10070796	0.87[EUR][1000 genomes]
rs10072379	0.83[ASN][1000 genomes]
rs10074435	0.92[EUR][1000 genomes]
rs10463637	0.87[EUR][1000 genomes]
rs10463640	0.89[EUR][1000 genomes]
rs11241169	0.88[EUR][1000 genomes]
rs11241170	0.88[EUR][1000 genomes]
rs11241173	0.92[EUR][1000 genomes]
rs11747636	0.83[ASN][1000 genomes]
rs11952093	0.90[EUR][1000 genomes]
rs11955149	0.88[EUR][1000 genomes]
rs13176097	0.83[ASN][1000 genomes]
rs13357891	0.87[EUR][1000 genomes]
rs1530508	0.87[EUR][1000 genomes]
rs1530509	0.87[EUR][1000 genomes]
rs1530510	0.87[EUR][1000 genomes]
rs2121162	0.87[EUR][1000 genomes]
rs2121163	0.87[EUR][1000 genomes]
rs2121164	0.86[EUR][1000 genomes]
rs2416291	0.86[EUR][1000 genomes]
rs28671308	0.92[EUR][1000 genomes]
rs28703859	0.91[EUR][1000 genomes]
rs338859	0.84[EUR][1000 genomes]
rs338870	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3934640	0.92[EUR][1000 genomes]
rs4269327	0.83[ASN][1000 genomes]
rs4455608	0.84[ASN][1000 genomes]
rs4958049	0.87[EUR][1000 genomes]
rs4958050	0.87[EUR][1000 genomes]
rs55655201	0.92[EUR][1000 genomes]
rs55813767	0.83[EUR][1000 genomes]
rs56034571	0.83[EUR][1000 genomes]
rs6594613	0.84[ASN][1000 genomes]
rs67793660	0.92[EUR][1000 genomes]
rs72793937	0.90[EUR][1000 genomes]
rs7378714	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7701118	0.84[ASN][1000 genomes]
rs7703562	0.83[ASN][1000 genomes]
rs9790874	0.92[EUR][1000 genomes]
rs9885457	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv599368	chr5:111399885-112032675	Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv882715	chr5:111836278-111894491	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
3	nsv882716	chr5:111848890-111894491	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:111891200-111899200	Weak transcription	Aorta	Aorta
2	chr5:111893200-111893400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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