Variant report

Variant	rs472630
Chromosome Location	chr11:84992547-84992548
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:84988076..84990491-chr11:84991343..84993778,2	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10501590	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs10792810	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs1400630	0.89[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap]
rs1517308	0.89[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1517310	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1517317	0.82[JPT][hapmap]
rs1914375	0.87[JPT][hapmap]
rs2000962	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs2203702	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs2449987	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs286045	0.84[ASN][1000 genomes]
rs286048	0.84[ASN][1000 genomes]
rs349077	0.81[CHB][hapmap];0.83[JPT][hapmap]
rs454388	0.84[ASN][1000 genomes]
rs471786	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4944512	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs530323	0.86[CHB][hapmap];0.87[JPT][hapmap];0.88[ASN][1000 genomes]
rs552017	0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs552373	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs556710	0.85[ASN][1000 genomes]
rs563788	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs580188	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs601857	1.00[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap]
rs660451	0.83[CHB][hapmap]
rs789600	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7935720	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs938727	0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs9734338	0.82[CHB][hapmap];0.87[JPT][hapmap]

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	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv898043	chr11:84895033-85148689	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv898044	chr11:84895033-85220773	ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 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	chr11:84967800-85019400	Weak transcription	Ovary	ovary
2	chr11:84974800-84998400	Weak transcription	HSMMtube	muscle
3	chr11:84992000-84992600	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr11:84992400-84992800	Enhancers	Primary B cells from peripheral blood	blood

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