Variant report

Variant	rs338843
Chromosome Location	chr5:111861758-111861759
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:111857753..111860186-chr5:111861145..111863385,2	K562	blood:

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11740414	0.92[CEU][hapmap];0.87[MEX][hapmap];0.80[TSI][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11745418	0.89[CEU][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11748780	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1422541	0.92[CEU][hapmap];0.91[MEX][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1445934	0.92[CEU][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1445935	0.92[CEU][hapmap];0.82[EUR][1000 genomes]
rs163456	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17134664	0.91[YRI][hapmap]
rs338842	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs338850	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs338854	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs338863	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs338864	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs338867	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs338869	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs338873	0.92[CEU][hapmap]
rs341289	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs341290	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs401722	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs430143	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs437318	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs445130	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4574588	0.80[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:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:111860600-111863400	Weak transcription	Adipose Nuclei	Adipose
2	chr5:111861000-111863400	Enhancers	Primary B cells from peripheral blood	blood
3	chr5:111861200-111868200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr5:111861600-111868000	Weak transcription	GM12878-XiMat	blood
5	chr5:111861600-111868200	Weak transcription	Primary B cells from cord blood	blood

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