Variant report

Variant	rs12633011
Chromosome Location	chr3:138938995-138938996
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	chr3:138931118..138932695-chr3:138937927..138940520,2	MCF-7	breast:
2	chr3:138937350..138939627-chr3:138942237..138943921,2	MCF-7	breast:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10804664	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11712639	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11719376	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11924028	0.89[EUR][1000 genomes]
rs12629284	0.80[ASN][1000 genomes]
rs12629323	0.80[ASN][1000 genomes]
rs12630019	0.80[ASN][1000 genomes]
rs12630565	0.83[ASN][1000 genomes]
rs12631107	0.80[ASN][1000 genomes]
rs12632107	0.81[CEU][hapmap]
rs12632544	0.82[ASN][1000 genomes]
rs12637124	0.81[ASN][1000 genomes]
rs12637329	0.80[ASN][1000 genomes]
rs12637397	0.82[ASN][1000 genomes]
rs12637601	0.82[ASN][1000 genomes]
rs12638754	0.80[ASN][1000 genomes]
rs12639299	0.80[ASN][1000 genomes]
rs12639501	0.80[ASN][1000 genomes]
rs13069303	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13074105	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13096665	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13097854	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13100625	0.85[EUR][1000 genomes]
rs17314607	0.89[EUR][1000 genomes]
rs4276214	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4521258	0.89[EUR][1000 genomes]
rs4894398	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4894399	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4894402	0.91[EUR][1000 genomes]
rs56947740	0.83[ASN][1000 genomes]
rs56970184	0.80[ASN][1000 genomes]
rs57178067	0.80[ASN][1000 genomes]
rs57625996	0.80[ASN][1000 genomes]
rs58210016	0.80[ASN][1000 genomes]
rs58710050	0.80[ASN][1000 genomes]
rs59021503	0.80[ASN][1000 genomes]
rs61379731	0.80[ASN][1000 genomes]
rs7623750	0.81[CEU][hapmap]
rs952389	0.89[EUR][1000 genomes]
rs955084	0.89[EUR][1000 genomes]
rs955085	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005167	chr3:138854490-138988546	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv536728	chr3:138854490-138988546	Enhancers Bivalent Enhancer Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	1 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	chr3:138936800-138944200	Weak transcription	Pancreas	Pancrea
2	chr3:138937000-138939600	Weak transcription	K562	blood
3	chr3:138937200-138939000	Weak transcription	Ovary	ovary
4	chr3:138938000-138944000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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