Variant report

Variant	rs966441
Chromosome Location	chr2:67940633-67940634
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	chr2:67939107..67941083-chr2:67942723..67945328,2	MCF-7	breast:
2	chr2:67934173..67935685-chr2:67939540..67941809,2	K562	blood:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10179159	0.90[ASN][1000 genomes]
rs10188512	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10191089	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10191839	0.85[CEU][hapmap]
rs10194664	0.85[CEU][hapmap]
rs10195055	0.82[CEU][hapmap]
rs10195947	0.86[CEU][hapmap]
rs10196069	0.86[CEU][hapmap]
rs10203976	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10203980	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10204184	0.86[CEU][hapmap]
rs10210853	0.89[CEU][hapmap]
rs11675630	0.81[EUR][1000 genomes]
rs11681312	0.81[EUR][1000 genomes]
rs11688644	0.85[CEU][hapmap]
rs13390163	0.92[ASN][1000 genomes]
rs13405830	0.80[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1367458	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1367461	0.84[CEU][hapmap]
rs1430773	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62155370	0.90[ASN][1000 genomes]
rs62155371	0.81[ASN][1000 genomes]
rs62155409	0.95[ASN][1000 genomes]
rs62155412	0.95[ASN][1000 genomes]
rs6717648	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6718114	0.80[EUR][1000 genomes]
rs724566	0.86[ASN][1000 genomes]
rs724567	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs737359	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7564631	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9309403	0.85[CEU][hapmap]
rs966443	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs974482	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][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	nsv534389	chr2:67388428-68225338	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
2	nsv1007345	chr2:67870225-67980094	Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv834250	chr2:67897722-68051532	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67939800-67944000	Weak transcription	NHLF	lung
2	chr2:67940000-67943600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr2:67940000-67945400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:67940400-67940800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:67940400-67940800	Enhancers	HMEC	breast

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