Variant report

Variant	rs2198451
Chromosome Location	chr11:59187545-59187546
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs1026320	0.87[EUR][1000 genomes]
rs10792232	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11601772	1.00[CEU][hapmap]
rs11602535	0.82[EUR][1000 genomes]
rs11602856	0.87[EUR][1000 genomes]
rs11604216	0.86[EUR][1000 genomes]
rs11605288	0.87[EUR][1000 genomes]
rs11605572	0.82[CEU][hapmap]
rs11606927	0.87[EUR][1000 genomes]
rs11606980	0.82[EUR][1000 genomes]
rs12417674	0.95[EUR][1000 genomes]
rs12418613	0.97[EUR][1000 genomes]
rs12419033	0.95[EUR][1000 genomes]
rs12419445	0.95[EUR][1000 genomes]
rs12420159	0.84[EUR][1000 genomes]
rs12420443	0.97[EUR][1000 genomes]
rs12420477	0.97[EUR][1000 genomes]
rs12785234	0.81[CEU][hapmap];0.86[EUR][1000 genomes]
rs12787182	0.82[EUR][1000 genomes]
rs12801196	0.97[EUR][1000 genomes]
rs12806497	0.98[EUR][1000 genomes]
rs12808401	0.98[EUR][1000 genomes]
rs12808731	0.97[EUR][1000 genomes]
rs1349777	0.81[CEU][hapmap];0.87[EUR][1000 genomes]
rs1453544	0.81[CEU][hapmap];0.85[EUR][1000 genomes]
rs1453547	0.81[CEU][hapmap];0.88[EUR][1000 genomes]
rs1453549	0.80[CEU][hapmap];0.87[EUR][1000 genomes]
rs1453550	0.81[CEU][hapmap];0.87[EUR][1000 genomes]
rs1453551	0.81[CEU][hapmap];0.87[EUR][1000 genomes]
rs1453552	0.86[EUR][1000 genomes]
rs1522757	1.00[YRI][hapmap]
rs1522759	0.95[CEU][hapmap];0.92[JPT][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1589600	0.80[EUR][1000 genomes]
rs1589601	0.97[EUR][1000 genomes]
rs1608210	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1608211	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1608212	0.80[EUR][1000 genomes]
rs17498652	0.97[EUR][1000 genomes]
rs17500478	0.85[EUR][1000 genomes]
rs17584022	0.82[EUR][1000 genomes]
rs17591107	0.81[CEU][hapmap];0.85[EUR][1000 genomes]
rs1851513	0.80[EUR][1000 genomes]
rs1879929	0.87[EUR][1000 genomes]
rs1955070	0.97[EUR][1000 genomes]
rs1972149	0.80[EUR][1000 genomes]
rs2123675	0.81[EUR][1000 genomes]
rs2123676	0.81[EUR][1000 genomes]
rs2167923	0.85[EUR][1000 genomes]
rs2219071	0.96[YRI][hapmap]
rs34037092	0.97[EUR][1000 genomes]
rs34387009	0.96[EUR][1000 genomes]
rs34730029	0.95[EUR][1000 genomes]
rs35630700	0.86[EUR][1000 genomes]
rs35872497	0.98[EUR][1000 genomes]
rs4938916	0.95[CEU][hapmap];0.92[JPT][hapmap]
rs61901576	0.86[EUR][1000 genomes]
rs61901620	0.85[EUR][1000 genomes]
rs61902489	0.98[EUR][1000 genomes]
rs61902558	0.99[EUR][1000 genomes]
rs61902559	0.86[EUR][1000 genomes]
rs61904569	0.91[EUR][1000 genomes]
rs61904597	0.95[EUR][1000 genomes]
rs7121582	0.80[EUR][1000 genomes]
rs7929008	0.91[EUR][1000 genomes]
rs7934882	0.97[EUR][1000 genomes]
rs7935959	0.87[EUR][1000 genomes]
rs9787928	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	nsv1050013	chr11:58394598-59221090	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv1046084	chr11:59034871-59314519	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1047952	chr11:59124719-59221606	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59186000-59190000	Weak transcription	Primary B cells from peripheral blood	blood
2	chr11:59187200-59188600	Weak transcription	Fetal Brain Male	brain
3	chr11:59187400-59187600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:59187400-59191200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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