Variant report

Variant	rs10133221
Chromosome Location	chr14:84496303-84496304
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:84496104..84497932-chr14:84499489..84501447,2	K562	blood:
2	chr14:84489726..84491906-chr14:84495009..84496588,2	MCF-7	breast:
3	chr14:84482307..84485229-chr14:84495468..84497989,2	MCF-7	breast:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10137482	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10139559	0.85[ASN][1000 genomes]
rs10148456	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10151367	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11851518	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12432538	0.83[ASN][1000 genomes]
rs12434360	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12435170	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12436496	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12587047	0.85[ASN][1000 genomes]
rs12587356	0.90[ASN][1000 genomes]
rs12589135	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12590331	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12590725	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17119380	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17119453	0.88[ASN][1000 genomes]
rs2183523	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28793601	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34326388	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4904151	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4904152	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4904153	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59954455	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7142351	0.92[ASN][1000 genomes]
rs7148040	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7155319	0.90[ASN][1000 genomes]
rs72701039	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7493561	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8007316	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8022878	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs952821	0.85[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1382	chr14:84487547-84532237	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84495600-84496400	Enhancers	HUVEC	blood vessel
2	chr14:84496000-84496400	Enhancers	Fetal Lung	lung
3	chr14:84496200-84496400	Enhancers	Adipose Nuclei	Adipose
4	chr14:84496200-84496400	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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