Variant report

Variant	rs338870
Chromosome Location	chr5:111878659-111878660
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10038874	0.83[EUR][1000 genomes]
rs10050436	0.85[EUR][1000 genomes]
rs10055787	0.85[EUR][1000 genomes]
rs10055908	0.83[EUR][1000 genomes]
rs10056032	0.85[EUR][1000 genomes]
rs10060366	0.83[EUR][1000 genomes]
rs10060474	0.83[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs10062535	0.83[EUR][1000 genomes]
rs10062917	0.85[EUR][1000 genomes]
rs10063938	0.85[EUR][1000 genomes]
rs10064939	0.83[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs10065523	0.85[EUR][1000 genomes]
rs10065629	0.85[EUR][1000 genomes]
rs10070796	0.85[EUR][1000 genomes]
rs10074435	0.80[EUR][1000 genomes]
rs10463637	0.85[EUR][1000 genomes]
rs10463640	0.80[EUR][1000 genomes]
rs11241169	0.85[EUR][1000 genomes]
rs11241170	0.85[EUR][1000 genomes]
rs11241172	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11241173	0.80[EUR][1000 genomes]
rs11955149	0.82[EUR][1000 genomes]
rs13357891	0.85[EUR][1000 genomes]
rs1530508	0.85[EUR][1000 genomes]
rs1530509	0.85[EUR][1000 genomes]
rs1530510	0.85[EUR][1000 genomes]
rs2121162	0.85[EUR][1000 genomes]
rs2121163	0.85[EUR][1000 genomes]
rs2121164	0.83[EUR][1000 genomes]
rs2416291	0.84[EUR][1000 genomes]
rs28671308	0.80[EUR][1000 genomes]
rs338859	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3934640	0.80[EUR][1000 genomes]
rs4958049	0.85[EUR][1000 genomes]
rs4958050	0.85[EUR][1000 genomes]
rs55655201	0.80[EUR][1000 genomes]
rs55813767	0.81[EUR][1000 genomes]
rs56034571	0.81[EUR][1000 genomes]
rs67793660	0.80[EUR][1000 genomes]
rs7378714	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9790874	0.80[EUR][1000 genomes]
rs9885457	0.81[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:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:111869600-111880000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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