Variant report

Variant	rs11724561
Chromosome Location	chr4:174894691-174894692
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10025010	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10050239	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11723453	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11734841	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11930283	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11932516	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4285061	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4289426	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4290874	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4299560	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4331760	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4501199	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4627836	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55801980	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60891530	0.83[EUR][1000 genomes]
rs62336579	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62336581	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62336609	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6814121	0.85[EUR][1000 genomes]
rs6815176	0.85[EUR][1000 genomes]
rs6818208	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6818217	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6830884	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6833109	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6845317	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6856702	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6858266	0.85[EUR][1000 genomes]
rs9998241	0.85[EUR][1000 genomes];1.00[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	nsv830154	chr4:174781983-174940640	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv527872	chr4:174873969-174908578	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:174894600-174894800	Enhancers	Aorta	Aorta

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